The document summarizes the development of the urogenital system from the early embryonic stages through fetal development. It describes how the urinary and genital systems develop from a common ridge in the intermediate mesoderm and initially share a common cavity, the cloaca. It then details the development of the pronephros, mesonephros, and metanephros kidney systems. It discusses the development of the permanent kidney from the metanephric mesoderm and ureteric bud. It also summarizes the development of the bladder, urethra, gonads, genital ducts, and external genitalia in both males and females.
This document discusses how various diseases can affect drug pharmacokinetics and metabolism. It covers effects of gastrointestinal, cardiac, renal, liver and thyroid disorders. Key points include:
- Renal and liver diseases can significantly impact drug absorption, distribution, metabolism and excretion. Dose adjustments are often needed.
- Cardiac failure can alter drug distribution and decrease elimination due to reduced hepatic and renal perfusion.
- Monitoring drug levels can help optimize therapy for individual patients, especially when inter-individual variability is high or clinical effects are difficult to assess. Close monitoring of response is important when prescribing for patients with organ dysfunction.
This document provides an overview of pharmacology and the use of drugs. It discusses:
- How drugs have advanced significantly from a limited number a century ago to thousands today, with further progress expected.
- The benefits drugs have provided to human health, but also the real risks of harm that must be considered given their potent effects.
- The basic duties of those prescribing drugs, which include restricting use only when warranted, carefully choosing appropriate drugs and doses, obtaining consent, and monitoring patients.
- Key considerations when developing a treatment plan, such as a patient's age, health conditions, the possibility of pregnancy, drug history, and personal beliefs and goals.
The cardiovascular system develops from progenitor heart cells that migrate to form the primary heart field (PHF). The PHF forms the atria, left ventricle and most of the right ventricle. The secondary heart field (SHF) forms the remainder of the right ventricle and outflow tract. These cells cluster to form the cardiogenic region and blood islands, which unite to form the heart tube. As the heart tube elongates due to SHF cell addition, it bends to form the cardiac loop. Septa then form to divide the heart into chambers, while cushions form valves and vessels. At birth, circulatory changes occur as the ductus arteriosus and foramen ovale close due
The document summarizes the anatomy of the abdominal wall and abdominal viscera. It describes the layers of the abdominal wall from the skin to the peritoneum. It details the five anterolateral muscles - external oblique, internal oblique, transversus abdominis, rectus abdominis, and pyramidalis. It also discusses the innervation, blood supply, and lymphatic drainage of the abdominal wall. Finally, it summarizes the peritoneal folds including the omenta, mesenteries, and ligaments that support the abdominal organs.
The abdominal aorta supplies the abdomen with blood vessels that branch into three main arteries:
(1) The celiac trunk which branches further into the left gastric, splenic, and common hepatic arteries.
(2) The superior mesenteric artery which supplies the small intestine and branches into jejunal, ileal, and colic arteries.
(3) The inferior mesenteric artery which supplies the descending colon, sigmoid colon, and rectum through branches like the left colic and superior rectal arteries.
Venous drainage of the abdominal organs is carried by the portal vein, formed by the union of the splenic and superior mesenteric veins. It delivers blood to the liver
The document summarizes key aspects of renal and urinary system anatomy and physiology. It describes the basic unit of the kidney, the nephron, and its components including the glomerulus and tubules. It explains renal circulation and the mechanisms of glomerular filtration, tubular reabsorption and secretion. Specific topics covered include regulation of sodium, water, glucose, potassium and urea, as well as the roles of diuretics and hormones like vasopressin and erythropoietin. The document concludes with descriptions of urine transport through the ureters and bladder filling and emptying during urination.
The document summarizes the development of the digestive system from the primitive gut tube. It describes how the gut tube is divided into the foregut, midgut, and hindgut. It explains how each section develops and gives rise to different parts of the digestive system. It also discusses the rotation and folding of the midgut and how the mesenteries that suspend the gut tube from the body wall develop and change throughout this process.
This document summarizes key points about pharmacology and drug use during pregnancy. It discusses how drugs can potentially harm the fetus, especially during organogenesis in the first trimester. Certain drugs like alcohol and cigarettes are definitely teratogenic. Most small drugs pass through the placenta. The document then covers organogenesis, fetal development, delivery, recognizing teratogenic drugs, and provides guidance on commonly used drug classes in pregnancy like analgesics, antibiotics, anti-epileptics, and cardiovascular drugs.
This document discusses how various diseases can affect drug pharmacokinetics and metabolism. It covers effects of gastrointestinal, cardiac, renal, liver and thyroid disorders. Key points include:
- Renal and liver diseases can significantly impact drug absorption, distribution, metabolism and excretion. Dose adjustments are often needed.
- Cardiac failure can alter drug distribution and decrease elimination due to reduced hepatic and renal perfusion.
- Monitoring drug levels can help optimize therapy for individual patients, especially when inter-individual variability is high or clinical effects are difficult to assess. Close monitoring of response is important when prescribing for patients with organ dysfunction.
This document provides an overview of pharmacology and the use of drugs. It discusses:
- How drugs have advanced significantly from a limited number a century ago to thousands today, with further progress expected.
- The benefits drugs have provided to human health, but also the real risks of harm that must be considered given their potent effects.
- The basic duties of those prescribing drugs, which include restricting use only when warranted, carefully choosing appropriate drugs and doses, obtaining consent, and monitoring patients.
- Key considerations when developing a treatment plan, such as a patient's age, health conditions, the possibility of pregnancy, drug history, and personal beliefs and goals.
The cardiovascular system develops from progenitor heart cells that migrate to form the primary heart field (PHF). The PHF forms the atria, left ventricle and most of the right ventricle. The secondary heart field (SHF) forms the remainder of the right ventricle and outflow tract. These cells cluster to form the cardiogenic region and blood islands, which unite to form the heart tube. As the heart tube elongates due to SHF cell addition, it bends to form the cardiac loop. Septa then form to divide the heart into chambers, while cushions form valves and vessels. At birth, circulatory changes occur as the ductus arteriosus and foramen ovale close due
The document summarizes the anatomy of the abdominal wall and abdominal viscera. It describes the layers of the abdominal wall from the skin to the peritoneum. It details the five anterolateral muscles - external oblique, internal oblique, transversus abdominis, rectus abdominis, and pyramidalis. It also discusses the innervation, blood supply, and lymphatic drainage of the abdominal wall. Finally, it summarizes the peritoneal folds including the omenta, mesenteries, and ligaments that support the abdominal organs.
The abdominal aorta supplies the abdomen with blood vessels that branch into three main arteries:
(1) The celiac trunk which branches further into the left gastric, splenic, and common hepatic arteries.
(2) The superior mesenteric artery which supplies the small intestine and branches into jejunal, ileal, and colic arteries.
(3) The inferior mesenteric artery which supplies the descending colon, sigmoid colon, and rectum through branches like the left colic and superior rectal arteries.
Venous drainage of the abdominal organs is carried by the portal vein, formed by the union of the splenic and superior mesenteric veins. It delivers blood to the liver
The document summarizes key aspects of renal and urinary system anatomy and physiology. It describes the basic unit of the kidney, the nephron, and its components including the glomerulus and tubules. It explains renal circulation and the mechanisms of glomerular filtration, tubular reabsorption and secretion. Specific topics covered include regulation of sodium, water, glucose, potassium and urea, as well as the roles of diuretics and hormones like vasopressin and erythropoietin. The document concludes with descriptions of urine transport through the ureters and bladder filling and emptying during urination.
The document summarizes the development of the digestive system from the primitive gut tube. It describes how the gut tube is divided into the foregut, midgut, and hindgut. It explains how each section develops and gives rise to different parts of the digestive system. It also discusses the rotation and folding of the midgut and how the mesenteries that suspend the gut tube from the body wall develop and change throughout this process.
This document summarizes key points about pharmacology and drug use during pregnancy. It discusses how drugs can potentially harm the fetus, especially during organogenesis in the first trimester. Certain drugs like alcohol and cigarettes are definitely teratogenic. Most small drugs pass through the placenta. The document then covers organogenesis, fetal development, delivery, recognizing teratogenic drugs, and provides guidance on commonly used drug classes in pregnancy like analgesics, antibiotics, anti-epileptics, and cardiovascular drugs.
The posterior abdominal region contains several important structures. The lumbar vertebrae and sacrum form the bony framework in the midline. The psoas major and minor muscles cover the sides of the lumbar vertebrae and attach to the femur. The quadratus lumborum muscles fill the space between rib 12 and the iliac crest laterally. The suprarenal glands are located superior to each kidney within the perinephric fat. Major blood vessels include the abdominal aorta, which bifurcates into the common iliac arteries at L4, and the inferior vena cava, which returns blood to the heart. Nerves in the region include the sympathetic trunks and splanchnic
The perineum is the diamond-shaped region between the pelvic outlet and the thighs. It is divided into an anterior urogenital triangle and a posterior anal triangle by an imaginary line between the ischial tuberosities. The anal triangle contains the external anal sphincter and is supplied by the inferior rectal branches of the pudendal nerve. The urogenital triangle contains erectile tissue that forms the clitoris or penis, as well as muscles and glands. The main blood supply is from the internal pudendal artery and its branches, while lymphatic drainage involves the superficial and deep inguinal nodes as well as internal iliac nodes.
Genetics is the study of genes, heredity, and inherited traits. Medical genetics deals with genetic causes of human diseases. The document discusses several types of chromosomal abnormalities including trisomies like Down syndrome, Edwards syndrome, and Patau syndrome. It also discusses sex chromosome abnormalities such as Turner syndrome, Klinefelter syndrome, and other conditions. Structural abnormalities of chromosomes including deletions, duplications, translocations, and microdeletions are also summarized. Chromosomal abnormalities are a major cause of genetic diseases and pregnancy complications.
This document summarizes several abdominal organs:
- The stomach is J-shaped and located in the epigastric, umbilical and hypochondrium regions. It has sections including the cardia, fundus, body, and pyloric part.
- The small intestine consists of the duodenum, jejunum, and ileum. The duodenum is C-shaped and adjacent to the pancreas. The jejunum is in the left upper quadrant and the ileum is in the right lower quadrant.
- The large intestine extends from the ileum to the anus. It includes the cecum, appendix, colon, rectum, and anal canal.
The respiratory system develops from the foregut. Around 4 weeks, lung buds appear and expand into the trachea and bronchi. Cartilage develops from pharyngeal arches while epithelium comes from endoderm. The trachea and lungs separate from the esophagus. Bronchial branching occurs through interactions between endoderm and surrounding mesoderm. Alveoli continue developing through pregnancy and after birth as surfactant production increases, allowing for breathing. Postnatally, alveoli and bronchioles continue multiplying to mature the lungs.
The cell cycle is a series of events that leads to cell duplication and division. It consists of four main phases - G1 phase where the cell grows, S phase where DNA is replicated, G2 phase where the cell prepares for division, and M phase where mitosis and cytokinesis occur resulting in two daughter cells. Progress through the cell cycle phases is tightly regulated by cyclin-dependent kinases and other proteins to ensure accurate DNA replication and cell division. Dysregulation of the cell cycle, as often happens in cancer, can lead to uncontrolled cell growth and division.
3. Cellular Organelles and Membrane Trafficking.pptxNkosinathiManana2
This document summarizes key aspects of membrane structure and function and cellular organelles. It describes how lipid bilayers form semipermeable membranes around cells and organelles, and how membrane proteins facilitate selective transport of molecules. It discusses the roles of pumps, carriers, and channels in moving substances across membranes using active or passive transport. Finally, it provides overviews of several important organelles, including their structures and functions, focusing on mitochondria and the endoplasmic reticulum.
The document summarizes the physiological changes that occur in a woman's body during pregnancy across multiple body systems. In the reproductive system, the uterus increases dramatically in size from 70g to 1100g by term as the myocyte arrangement changes. Blood flow to the uterus and placenta increases substantially to support fetal growth. The cervix softens and other changes occur to facilitate delivery. Metabolic changes include increased weight gain of 12.5kg on average, water retention of 3.5L for the fetus and fluids, and increased protein, carbohydrate, fat, electrolyte and mineral needs to support the growing fetus and maternal reserves. Hematological changes include a 40-45% increase in blood volume by the third trimester
The pelvis consists of bones that form the pelvic cavity and outlet. The bones include the sacrum, coccyx, and two innominate bones formed from the fusion of the ilium, pubis, and ischium. These bones articulate at the sacroiliac joints and pubic symphysis. The pelvic cavity contains organs and is divided into the lesser pelvis and greater pelvis. The pelvic outlet is bounded by ligaments and muscles and contains three apertures.
Gametogenesis is the process by which germ cells undergo meiosis and differentiation to form gametes. Primordial germ cells migrate to the developing gonads, where they differentiate into male or female gametes. In females, primordial germ cells become oogonia then oocytes through oogenesis. In males, they become spermatogonia and undergo spermatogenesis to become spermatozoa. Both processes involve mitosis, meiosis, and cellular changes to produce haploid gametes from diploid germ cells. Fertilization restores the diploid number through the union of male and female gametes.
The document summarizes key developments during the 2nd week (days 8-13) of embryonic development:
- By day 8, the blastocyst is partially embedded and cells in the cytotrophoblast migrate and fuse to form the syncytiotrophoblast. The embryoblast also differentiates into the hypoblast and epiblast layers.
- By days 11-12, the blastocyst is completely embedded and the syncytiotrophoblast forms lacunar spaces that connect to maternal blood sinusoids, establishing uteroplacental circulation. Extraembryonic mesoderm also develops.
- By day 13, the implantation site has usually healed and the trophoblast develops villous structures
The embryonic stage occurs from 3-8 weeks of development. During this stage, the three germ layers (ectoderm, mesoderm, endoderm) give rise to major organ systems. By the end of the embryonic period, the main organ systems are established. The ectoderm forms the central nervous system and skin/hair/nails. Neural crest cells migrate from the ectoderm to form many structures. The mesoderm forms muscles, bones, and the circulatory system. The endoderm forms the lining of the digestive tract and respiratory system. Neurulation occurs during the third week, forming the neural tube which will become the brain and spinal cord.
This document summarizes key aspects of gastrulation and early embryonic development that occur during the third week. It describes how gastrulation establishes the three germ layers through cell migration along the primitive streak. It also discusses the formation of structures like the notochord and establishment of the body axes. Finally, it provides an overview of trophoblast development and how the chorionic cavity enlarges and the embryo attaches via the connecting stalk.
Embryology is the study of the complex process of development from a single cell to a baby. It includes investigations of the molecular, cellular, and structural factors that contribute to organism formation. The first 8 weeks of human development is called embryogenesis, where organs form. From then until birth is the fetal period. Studying causes of birth defects is called teratology. There are approximately 23,000 genes in the human genome, but gene expression is regulated at several levels, including transcription, messenger RNA, and translation, which results in over 5 times as many proteins. Organ formation involves induction, where one group of cells causes another to change fate, and competence, the ability to respond. Many interactions occur between epithelial and me
This document summarizes the processes of gametogenesis and ovulation. It discusses folliculogenesis, from primordial follicles to the pre-ovulatory development of the dominant follicle. The luteal phase and corpus luteum formation after ovulation is also described. Finally, it provides an overview of the hormonal regulation of the menstrual cycle by the hypothalamic-pituitary-ovarian axis, and the correlated endometrial changes through the proliferative, secretory and menstrual phases.
The pelvic floor is formed by the pelvic diaphragm and the perineal membrane. The pelvic diaphragm consists of the levator ani and coccygeus muscles, which attach superiorly to the pelvic wall. The levator ani muscles originate from the pelvic wall and join together in the midline, forming a U-shaped defect anteriorly. The coccygeus muscles are triangular shaped and overlie the sacrum and coccyx. The perineal membrane is a thick fascia attached to the pubic arch, with a thin space above it called the deep perineal pouch containing muscles and vessels. The perineal body is a connective
The male reproductive system consists of both internal and external components. Internally, it includes the testes, epididymis, ductus deferens, seminal vesicles, ejaculatory ducts, prostate and part of the urethra. Externally it includes the scrotum and penis. Sperm are produced in the testes and travel through the epididymis, ductus deferens and ejaculatory duct to mix with fluids from the seminal vesicles and prostate to form semen, which is ejaculated through the urethra. The scrotum houses the testes and maintains the optimal temperature for sperm production.
The document summarizes key stages in human fertilization and early embryonic development. It describes:
1) How sperm capacitation and the acrosome reaction allow sperm to penetrate the zona pellucida and fuse with the egg.
2) The formation of pronuclei and how the zygote undergoes cell division to become a morula and then a blastocyst.
3) The process of blastocyst implantation in the uterine lining and how trophoblast cells mediate attachment to the endometrium.
The pituitary gland lies at the base of the brain and coordinates many endocrine glands. It has an anterior and posterior lobe. The anterior lobe secretes hormones like TSH, ACTH, LH, and FSH which respond to signals from the hypothalamus. The posterior lobe stores and releases oxytocin and vasopressin from nerve cell bodies in the hypothalamus. The anterior pituitary contains five major cell types that secrete different hormones like growth hormone, prolactin, and gonadotropins.
The document summarizes key aspects of fetal and placental development from 8 weeks gestation through birth. It describes how the fetus grows in length and weight over time. The placenta facilitates nutrient and gas exchange between mother and fetus. As pregnancy progresses, the placenta enlarges and the fetal membranes thin to increase exchange. The umbilical cord contains the vessels connecting the fetus and placenta. Amniotic fluid volume increases throughout pregnancy, providing cushioning and allowing fetal movement.
The urinary system develops from the intermediate mesoderm and includes three successive kidney structures - the pronephros, mesonephros, and metanephros. The metanephros forms the permanent kidneys. It develops from the ureteric bud penetrating the metanephric mesoderm and inducing nephron formation. The kidneys ascend into the abdominal cavity during development and become fully functional by 12 weeks of gestation. The urinary bladder and urethra also develop from the intermediate mesoderm through partitioning of the cloaca.
1. The urinary and genital systems develop from a common intermediate mesoderm and initially share a common cavity called the cloaca.
2. The kidneys develop through three successive stages - the pronephros, mesonephros, and metanephros - with the metanephros forming the permanent kidneys.
3. The ureters develop from the mesonephric ducts and later join the bladder, which develops from the urogenital sinus. The bladder remains connected to the umbilicus by the urachus in early development.
The posterior abdominal region contains several important structures. The lumbar vertebrae and sacrum form the bony framework in the midline. The psoas major and minor muscles cover the sides of the lumbar vertebrae and attach to the femur. The quadratus lumborum muscles fill the space between rib 12 and the iliac crest laterally. The suprarenal glands are located superior to each kidney within the perinephric fat. Major blood vessels include the abdominal aorta, which bifurcates into the common iliac arteries at L4, and the inferior vena cava, which returns blood to the heart. Nerves in the region include the sympathetic trunks and splanchnic
The perineum is the diamond-shaped region between the pelvic outlet and the thighs. It is divided into an anterior urogenital triangle and a posterior anal triangle by an imaginary line between the ischial tuberosities. The anal triangle contains the external anal sphincter and is supplied by the inferior rectal branches of the pudendal nerve. The urogenital triangle contains erectile tissue that forms the clitoris or penis, as well as muscles and glands. The main blood supply is from the internal pudendal artery and its branches, while lymphatic drainage involves the superficial and deep inguinal nodes as well as internal iliac nodes.
Genetics is the study of genes, heredity, and inherited traits. Medical genetics deals with genetic causes of human diseases. The document discusses several types of chromosomal abnormalities including trisomies like Down syndrome, Edwards syndrome, and Patau syndrome. It also discusses sex chromosome abnormalities such as Turner syndrome, Klinefelter syndrome, and other conditions. Structural abnormalities of chromosomes including deletions, duplications, translocations, and microdeletions are also summarized. Chromosomal abnormalities are a major cause of genetic diseases and pregnancy complications.
This document summarizes several abdominal organs:
- The stomach is J-shaped and located in the epigastric, umbilical and hypochondrium regions. It has sections including the cardia, fundus, body, and pyloric part.
- The small intestine consists of the duodenum, jejunum, and ileum. The duodenum is C-shaped and adjacent to the pancreas. The jejunum is in the left upper quadrant and the ileum is in the right lower quadrant.
- The large intestine extends from the ileum to the anus. It includes the cecum, appendix, colon, rectum, and anal canal.
The respiratory system develops from the foregut. Around 4 weeks, lung buds appear and expand into the trachea and bronchi. Cartilage develops from pharyngeal arches while epithelium comes from endoderm. The trachea and lungs separate from the esophagus. Bronchial branching occurs through interactions between endoderm and surrounding mesoderm. Alveoli continue developing through pregnancy and after birth as surfactant production increases, allowing for breathing. Postnatally, alveoli and bronchioles continue multiplying to mature the lungs.
The cell cycle is a series of events that leads to cell duplication and division. It consists of four main phases - G1 phase where the cell grows, S phase where DNA is replicated, G2 phase where the cell prepares for division, and M phase where mitosis and cytokinesis occur resulting in two daughter cells. Progress through the cell cycle phases is tightly regulated by cyclin-dependent kinases and other proteins to ensure accurate DNA replication and cell division. Dysregulation of the cell cycle, as often happens in cancer, can lead to uncontrolled cell growth and division.
3. Cellular Organelles and Membrane Trafficking.pptxNkosinathiManana2
This document summarizes key aspects of membrane structure and function and cellular organelles. It describes how lipid bilayers form semipermeable membranes around cells and organelles, and how membrane proteins facilitate selective transport of molecules. It discusses the roles of pumps, carriers, and channels in moving substances across membranes using active or passive transport. Finally, it provides overviews of several important organelles, including their structures and functions, focusing on mitochondria and the endoplasmic reticulum.
The document summarizes the physiological changes that occur in a woman's body during pregnancy across multiple body systems. In the reproductive system, the uterus increases dramatically in size from 70g to 1100g by term as the myocyte arrangement changes. Blood flow to the uterus and placenta increases substantially to support fetal growth. The cervix softens and other changes occur to facilitate delivery. Metabolic changes include increased weight gain of 12.5kg on average, water retention of 3.5L for the fetus and fluids, and increased protein, carbohydrate, fat, electrolyte and mineral needs to support the growing fetus and maternal reserves. Hematological changes include a 40-45% increase in blood volume by the third trimester
The pelvis consists of bones that form the pelvic cavity and outlet. The bones include the sacrum, coccyx, and two innominate bones formed from the fusion of the ilium, pubis, and ischium. These bones articulate at the sacroiliac joints and pubic symphysis. The pelvic cavity contains organs and is divided into the lesser pelvis and greater pelvis. The pelvic outlet is bounded by ligaments and muscles and contains three apertures.
Gametogenesis is the process by which germ cells undergo meiosis and differentiation to form gametes. Primordial germ cells migrate to the developing gonads, where they differentiate into male or female gametes. In females, primordial germ cells become oogonia then oocytes through oogenesis. In males, they become spermatogonia and undergo spermatogenesis to become spermatozoa. Both processes involve mitosis, meiosis, and cellular changes to produce haploid gametes from diploid germ cells. Fertilization restores the diploid number through the union of male and female gametes.
The document summarizes key developments during the 2nd week (days 8-13) of embryonic development:
- By day 8, the blastocyst is partially embedded and cells in the cytotrophoblast migrate and fuse to form the syncytiotrophoblast. The embryoblast also differentiates into the hypoblast and epiblast layers.
- By days 11-12, the blastocyst is completely embedded and the syncytiotrophoblast forms lacunar spaces that connect to maternal blood sinusoids, establishing uteroplacental circulation. Extraembryonic mesoderm also develops.
- By day 13, the implantation site has usually healed and the trophoblast develops villous structures
The embryonic stage occurs from 3-8 weeks of development. During this stage, the three germ layers (ectoderm, mesoderm, endoderm) give rise to major organ systems. By the end of the embryonic period, the main organ systems are established. The ectoderm forms the central nervous system and skin/hair/nails. Neural crest cells migrate from the ectoderm to form many structures. The mesoderm forms muscles, bones, and the circulatory system. The endoderm forms the lining of the digestive tract and respiratory system. Neurulation occurs during the third week, forming the neural tube which will become the brain and spinal cord.
This document summarizes key aspects of gastrulation and early embryonic development that occur during the third week. It describes how gastrulation establishes the three germ layers through cell migration along the primitive streak. It also discusses the formation of structures like the notochord and establishment of the body axes. Finally, it provides an overview of trophoblast development and how the chorionic cavity enlarges and the embryo attaches via the connecting stalk.
Embryology is the study of the complex process of development from a single cell to a baby. It includes investigations of the molecular, cellular, and structural factors that contribute to organism formation. The first 8 weeks of human development is called embryogenesis, where organs form. From then until birth is the fetal period. Studying causes of birth defects is called teratology. There are approximately 23,000 genes in the human genome, but gene expression is regulated at several levels, including transcription, messenger RNA, and translation, which results in over 5 times as many proteins. Organ formation involves induction, where one group of cells causes another to change fate, and competence, the ability to respond. Many interactions occur between epithelial and me
This document summarizes the processes of gametogenesis and ovulation. It discusses folliculogenesis, from primordial follicles to the pre-ovulatory development of the dominant follicle. The luteal phase and corpus luteum formation after ovulation is also described. Finally, it provides an overview of the hormonal regulation of the menstrual cycle by the hypothalamic-pituitary-ovarian axis, and the correlated endometrial changes through the proliferative, secretory and menstrual phases.
The pelvic floor is formed by the pelvic diaphragm and the perineal membrane. The pelvic diaphragm consists of the levator ani and coccygeus muscles, which attach superiorly to the pelvic wall. The levator ani muscles originate from the pelvic wall and join together in the midline, forming a U-shaped defect anteriorly. The coccygeus muscles are triangular shaped and overlie the sacrum and coccyx. The perineal membrane is a thick fascia attached to the pubic arch, with a thin space above it called the deep perineal pouch containing muscles and vessels. The perineal body is a connective
The male reproductive system consists of both internal and external components. Internally, it includes the testes, epididymis, ductus deferens, seminal vesicles, ejaculatory ducts, prostate and part of the urethra. Externally it includes the scrotum and penis. Sperm are produced in the testes and travel through the epididymis, ductus deferens and ejaculatory duct to mix with fluids from the seminal vesicles and prostate to form semen, which is ejaculated through the urethra. The scrotum houses the testes and maintains the optimal temperature for sperm production.
The document summarizes key stages in human fertilization and early embryonic development. It describes:
1) How sperm capacitation and the acrosome reaction allow sperm to penetrate the zona pellucida and fuse with the egg.
2) The formation of pronuclei and how the zygote undergoes cell division to become a morula and then a blastocyst.
3) The process of blastocyst implantation in the uterine lining and how trophoblast cells mediate attachment to the endometrium.
The pituitary gland lies at the base of the brain and coordinates many endocrine glands. It has an anterior and posterior lobe. The anterior lobe secretes hormones like TSH, ACTH, LH, and FSH which respond to signals from the hypothalamus. The posterior lobe stores and releases oxytocin and vasopressin from nerve cell bodies in the hypothalamus. The anterior pituitary contains five major cell types that secrete different hormones like growth hormone, prolactin, and gonadotropins.
The document summarizes key aspects of fetal and placental development from 8 weeks gestation through birth. It describes how the fetus grows in length and weight over time. The placenta facilitates nutrient and gas exchange between mother and fetus. As pregnancy progresses, the placenta enlarges and the fetal membranes thin to increase exchange. The umbilical cord contains the vessels connecting the fetus and placenta. Amniotic fluid volume increases throughout pregnancy, providing cushioning and allowing fetal movement.
The urinary system develops from the intermediate mesoderm and includes three successive kidney structures - the pronephros, mesonephros, and metanephros. The metanephros forms the permanent kidneys. It develops from the ureteric bud penetrating the metanephric mesoderm and inducing nephron formation. The kidneys ascend into the abdominal cavity during development and become fully functional by 12 weeks of gestation. The urinary bladder and urethra also develop from the intermediate mesoderm through partitioning of the cloaca.
1. The urinary and genital systems develop from a common intermediate mesoderm and initially share a common cavity called the cloaca.
2. The kidneys develop through three successive stages - the pronephros, mesonephros, and metanephros - with the metanephros forming the permanent kidneys.
3. The ureters develop from the mesonephric ducts and later join the bladder, which develops from the urogenital sinus. The bladder remains connected to the umbilicus by the urachus in early development.
Embryology Course IX - Urogenital SystemRawa Muhsin
This session discusses the development of the urogenital system and includes:
1. Development of the kidneys and ureters
2. Development of the bladder and urethra
3. Development of the gonads and genital ducts
4. Development of the external genitalia
The document summarizes the development of the urogenital system. It describes how the urinary and genital systems develop from a common intermediate mesoderm and cloaca. The three kidney systems - pronephros, mesonephros, and metanephros - develop sequentially. The metanephros forms the permanent kidney. The urinary bladder, urethra, and genital structures like the uterus, vagina, and external genitalia also develop from the intermediate mesoderm and urogenital sinus. The kidneys ascend to their final position in the lumbar region during development.
The document summarizes the development of the female reproductive system. It begins with the formation of the genital ridge in the intermediate mesoderm at 3 weeks. At 5-6 weeks, primordial germ cells form the indifferent gonad. In the absence of the Y chromosome, the gonad develops into an ovary with cortical cords and primordial follicles. The ovaries descend into the pelvis guided by the gubernaculum. Meanwhile, the paramesonephric ducts form the fallopian tubes, uterus and upper vagina. The vagina develops from the sinovaginal bulbs and vaginal plate. Remnants of the mesonephric ducts include the epoophoron and
This document summarizes the development of the urinary system and suprarenal gland. It discusses how they both originate from the intermediate mesoderm. It describes the development of the pronephros, mesonephros, and metanephros, which give rise to the permanent kidneys. It also discusses the development of the ureters, bladder, and collecting system from the ureteric bud. Finally, it summarizes how the suprarenal glands develop from mesenchyme and neural crest cells to form the cortex and medulla, respectively.
The urinary system develops from the intermediate mesoderm. Three sets of kidneys develop in embryos - the pronephros, mesonephros, and metanephros. The metanephros forms the permanent kidneys. The kidneys begin developing as the ureteric bud invades the metanephrogenic blastema and undergoes branching. This induces nephron formation from the blastema. The kidneys initially form near the sacrum but ascend into the abdomen as the embryo grows. The bladder develops from the urogenital sinus and remains connected to the allantois until constriction forms the urachus. The urethra epithelium derives from endoderm except for
This document discusses renal embryology and kidney development. It begins by outlining the three main stages of kidney development - the pronephros, mesonephros, and metanephros. It then provides details on the development of each of these stages, including how they form from the intermediate mesoderm and their roles. The document also discusses genetic factors involved in kidney differentiation, abnormal kidney development including anomalies in number and position, and applied aspects such as hereditary polycystic kidneys.
The document summarizes the embryological development of the genitourinary tract. It discusses that the kidneys, bladder, ureters, and genital/reproductive tracts all originate from the intermediate mesoderm. It describes the development of the pronephros, mesonephros, and metanephros kidney systems, as well as the development of the bladder, ureters, and genital ridges that form the gonads and ducts. Key interactions between epithelial and mesenchymal tissues regulate the formation and differentiation of these structures in a highly coordinated process.
1. The genital system develops from the intermediate mesoderm, celomic epithelium, and part of the cloaca. Genetic sex is established at fertilization as XY or XX.
2. Between 4-12 weeks, the genital ridges develop into testes or ovaries depending on the presence of SRY gene on Y chromosome. This gene encodes TDF which leads to male development.
3. The genital ducts initially consist of the mesonephric and paramesonephric ducts. In males, the mesonephric ducts form the epididymis, vas deferens, and ejaculatory duct while the paramesonephric ducts regress. In females
The document discusses the male reproductive system and spermatogenesis. It describes the major structures of the male reproductive system including the testes, duct system, and accessory glands. It then focuses on the microscopic structure and function of the seminiferous tubules where spermatogenesis occurs. Spermatogenesis is the process by which spermatogonia differentiate and develop into spermatozoa through spermatocytogenesis, meiosis, and spermiogenesis within the seminiferous tubules of the testes. Sertoli and germ cells are also described in detail for their roles in supporting spermatogenesis.
1. The document describes the development of the urinary and genital systems from the intermediate mesoderm.
2. Three kidney systems form sequentially - the pronephros, mesonephros, and metanephros. The metanephros persists to form the permanent kidneys.
3. The kidneys ascend from the pelvic region to the abdomen during development. The urinary bladder and urethra develop from the urogenital sinus which divides the cloaca.
The development of the female genital system is determined at fertilization by the presence of two X chromosomes. In female embryos, the primitive sex cords dissociate and are replaced by the ovarian medulla and cortex. The paramesonephric ducts develop into the uterus, fallopian tubes, and upper vagina, while the sinovaginal bulbs form the lower vagina. Defects can occur if the paramesonephric ducts fail to fuse properly, resulting in conditions like a septate, bicornuate, or didelphys uterus. The genital tubercle forms the clitoris and genital swellings become the labia, with the urethral folds
1. The document describes the development of the male and female genital systems from early embryonic stages through formation of the internal and external genitalia.
2. Key events include formation of the genital ridges which develop into testes in males and ovaries in females, descent of the testes into the scrotum, development of the duct systems including the vas deferens and epididymis in males and Mullerian duct regression leading to formation of the uterus and vagina in females.
3. External genitalia develop from the genital tubercle and swellings, with the penis and scrotum forming in males and clitoris, labia, and vagina developing in females.
Fetal monitoring aims to assess fetal wellbeing during pregnancy and labor. This document provides guidelines for interpreting cardiotocography (CTG) traces and responding to patterns. CTGs should consider gestational age, fetal growth, movements, and any conditions affecting fetal wellbeing. Antenatally, reduced fetal movements or abnormal fundal height measurements may warrant further assessment. During labor, CTG is recommended for high-risk pregnancies and can identify non-reassuring patterns like late decelerations indicating possible hypoxia. Interpretation requires evaluating baseline rate, variability, decelerations, and accelerations in the context of the clinical situation.
This document provides guidance on antenatal care. It discusses the importance of preconception care, screening and risk assessment during pregnancy, and the essential components of antenatal visits. The goals of antenatal care are to ensure the best outcomes for women and babies by screening for problems, assessing risk, treating issues, providing medications and information. Key aspects covered include taking a medical history, conducting physical exams, estimating gestation, performing essential screening tests, discussing medications and vaccines, creating a management plan, and covering topics for subsequent routine prenatal visits.
This document provides guidelines for preventing mother-to-child transmission of HIV (PMTCT) in antenatal care settings. There are four key elements of PMTCT care: primary HIV prevention, preventing unintended pregnancies among HIV+ women, preventing transmission from mother to child, and treatment/support for HIV+ women and their families. The goals of PMTCT in antenatal care are to identify all HIV+ women, provide same-day ART to optimize health and prevent transmission, and ensure viral suppression through treatment. All pregnant women should be tested for HIV and receive counseling. HIV+ women initiate lifelong ART regardless of CD4 count or clinical stage, while HIV- women receive repeat testing during pregnancy and breastfeeding.
This document provides guidance on performing and managing caesarean deliveries. It discusses:
- The need for caesarean delivery capabilities 24/7 at district hospitals and ability to perform emergency c-sections within 1 hour.
- Testing fetal lung maturity before elective c-sections if gestational age is uncertain.
- Preparation steps like consent, blood availability, and ensuring an experienced surgeon.
- Precautions against hemorrhage like oxytocin administration and careful surgical technique.
- Managing hemorrhage through measures like massaging the uterus, giving uterotonics, exploring for bleeding sources, and considering compression sutures.
- Postoperative orders around analgesia, fluids, thrombosis
Induction of labour is the artificial initiation of labour to achieve a vaginal delivery. Common indications include post-term pregnancy, hypertension disorders, and pre-labour rupture of membranes. The document discusses assessing the need for induction and balancing risks to the mother and baby. It provides guidance on methods for induction including membranes sweeping, prostaglandins, misoprostol, and oxytocin administration. Risks like uterine hyperstimulation are addressed. Special considerations for fetal demise, ruptured membranes, and scarred uteruses are also covered.
This document provides guidance on diagnosing and treating infections during pregnancy and the postpartum period. It discusses abnormal vaginal discharge, sexually transmitted infections like candidiasis, gonorrhea, chlamydia and trichomoniasis. It also addresses genital warts, ulcers, syphilis, urinary tract infections, acute pyelonephritis, and malaria. For each condition, it describes signs and symptoms, recommended testing, and treatment guidelines. It emphasizes treating sexually transmitted infections syndromically and the importance of notifying partners for examination and treatment.
This document provides guidelines for managing medical disorders in pregnancy, including anemia, diabetes mellitus, and cardiac disease. For anemia, it outlines screening, prevention, and treatment protocols. It describes gestational and pregestational diabetes and their management. For cardiac disease, it discusses referral criteria and managing labor and delivery for high-risk patients. The overall aim is to provide optimal care for both mother and baby's health outcomes.
1) Tuberculosis (TB) is a major cause of maternal mortality in South Africa. All pregnant women, especially those with HIV, should be screened for TB at antenatal visits.
2) Symptom screening involves asking about cough, fever, night sweats, and weight loss. A TB test (GeneXpert) is also required for pregnant women with new HIV diagnoses or known HIV.
3) If TB is diagnosed, treatment should begin promptly according to national guidelines. For drug-resistant TB, consultation with infectious disease specialists is recommended due to high mortality risk.
1) Bleeding in early pregnancy, defined as before 22 weeks, can be caused by miscarriage, ectopic pregnancy, molar pregnancy, or other issues. A rapid assessment including vital signs and exam is needed.
2) Miscarriages are categorized as safe, unsafe, threatening, inevitable, incomplete, or septic and management depends on the category and gestational age. Manual vacuum aspiration is preferred for evacuating the uterus under 16 weeks.
3) Post-miscarriage care involves screening for physical and mental health issues, providing counseling and information, and discussing family planning options.
Pregnant and postpartum women with COVID-19 should receive supportive care. While pregnant women are not more likely to get infected, those who do contract COVID-19, especially in the third trimester, are at higher risk of severe outcomes. COVID-19 testing criteria are the same for pregnant women as non-pregnant adults. Preventative measures include vaccination, masks, distancing, and hygiene. COVID-19 vaccination is recommended in pregnancy to protect both mother and baby. Mild cases can be isolated at home but moderate or severe cases require hospital admission. Mode of delivery depends on obstetric needs and maternal stability.
This document provides guidance on the management of antepartum haemorrhage (APH), or bleeding during pregnancy prior to delivery. It discusses causes of APH including placental abnormalities, infections, trauma, and unknown causes. It provides recommendations for emergency management at clinics, community health centers, and hospitals. Specific guidance is given for managing placenta praevia, abruptio placentae, and APH of unknown origin. Recommendations include IV fluids, blood transfusions, ultrasound exams, monitoring vital signs, and determining need for transfer or delivery.
Hypertensive disorders in pregnancy (HDP) are a common cause of maternal and infant health problems and death. HDP include gestational hypertension, preeclampsia, and eclampsia. Risk factors include being young, older than 35, having previous HDP, obesity, diabetes, or kidney disease. Symptoms of severe preeclampsia include headaches, vision issues, low platelets, elevated liver enzymes, pain in the upper right abdomen, HELLP syndrome, or high creatinine. All pregnant people should take calcium and those at higher risk may benefit from low-dose aspirin. HDP requires frequent monitoring, control of blood pressure, delivery by 38 weeks for gestational hypertension or earlier for pre
This document discusses gender-based violence and provides guidance for health workers in responding to GBV. It begins by defining GBV and noting that 1 in 4 women in South Africa experience GBV during pregnancy. It then outlines the negative health impacts of untreated GBV for women and children. The document describes possible signs that a woman is experiencing violence and provides a screening tool for health workers. It provides guidance on first line support, safety planning, and self-care for health workers responding to disclosures of GBV.
The document summarizes various abnormalities that can occur during labour and their management. It discusses prolonged latent phase of labour, poor progress in the active phase, meconium staining of amniotic fluid, prolonged second stage of labour, vacuum extraction, fetal distress, cord prolapse, and shoulder dystocia. For each issue, it provides details on how to assess and manage the situation, including administering drugs, changing positioning, accelerating delivery, or transferring to a hospital if needed. The goal is to safely resolve any problems and deliver a healthy baby.
1. The document discusses fetal maturity and intrauterine growth restriction (IUGR), including definitions, clinical symptoms, signs, biochemical markers, and fetal maturity tests. Fetal maturity tests assess surfactant levels in amniotic fluid to predict risk of respiratory distress syndrome in newborns.
2. IUGR is defined as fetal weight below the 10th percentile and can be symmetric or asymmetric, early or late onset. It increases risks of complications. Management depends on gestational age and Doppler ultrasound results, with delivery generally between 34-37 weeks.
3. There is no worldwide consensus on specific management strategies for IUGR, and guidelines from organizations like RCOG and ACOG have some differences.
The document discusses how the fetus is able to survive as a semi-allograft within the mother's uterus despite having different genetic material. It was first proposed in 1953 that the fetus is able to evade maternal immune detection through lack of fetal antigen expression or maternal lymphocyte suppression. The document then explores various mechanisms by which the fetal-maternal interface avoids rejection, including lack of MHC class I expression on trophoblast cells, shifts in maternal immune cell profiles toward anti-inflammatory responses, and expression of inhibitory ligands on trophoblasts. Immune cells in both the peripheral maternal system and local decidua are adapted to tolerate the semi-allogeneic fetus through these various mechanisms.
Teratology is the study of birth defects and their causes. Some key points:
- Around 5% of newborns have a detectable birth defect, though the cause is unknown for 70% of cases. Less than 1% are due to medications.
- Teratogens are agents that cause permanent changes to embryonic or fetal development, and can cause malformations (teratogen), altered growth (trophogen), or interference with organ maturation (hadegen).
- Studying teratogenicity in humans is difficult due to ethical concerns, so animal studies are also used but not definitive. Counseling women exposed to potential teratogens is important to avoid anxiety.
- Amniotic fluid serves several important roles in fetal development including allowing movement, swallowing, breathing and protecting the fetus.
- The normal volume of amniotic fluid increases throughout pregnancy reaching around 800mL by the mid-third trimester. Abnormally low (oligohydramnios) or high (hydramnios) volumes can occur.
- Hydramnios, which complicates 1-2% of pregnancies, has many potential causes including fetal anomalies, diabetes or infections. It can lead to pregnancy complications like cesarean delivery. Oligohydramnios also has various causes like renal abnormalities and medications and is associated with adverse outcomes such as pulmonary hypoplasia
This document discusses various fetal disorders, focusing on fetal anemia, hydrops fetalis, and thrombocytopenia. It describes the main causes of fetal anemia as red blood cell alloimmunization and various infections. Doppler evaluation and fetal blood sampling are used to identify and monitor anemia. Left untreated, anemia can lead to heart failure, hydrops, and death. However, intrauterine transfusions have dramatically improved survival rates. Hydrops fetalis refers to fluid accumulation and can result from immune or nonimmune causes. For immune hydrops, the main cause is red blood cell alloimmunization, while aneuploidy and infections are common nonimmune causes. Thrombocytopenia can
This document provides an overview of prenatal diagnosis. It discusses how major congenital abnormalities are identified in 2-3% of pregnancies and are a leading cause of infant death. Prenatal diagnosis aims to identify fetal malformations, disruptions, and genetic syndromes to improve counseling. Structural abnormalities can develop through malformation, deformation, or disruption. Neural tube defects are among the most common birth defects. Maternal serum screening for alpha-fetoprotein is an established screening test for neural tube defects. Advances in screening include first trimester screening using nuchal translucency and serum markers, as well as cell-free DNA screening. Sonographic screening can identify soft markers and structural abnormalities. Pregnancies at
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Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
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2. Intro
• The urogenital system can be divided into two entirely different
components: the urinary system and the genital system
• Embryologically and anatomically, however, they are intimately
interwoven
• Both develop from a common mesodermal ridge (intermediate
mesoderm)
• Initially, the excretory ducts of both systems enter a common cavity,
the cloaca
3. Kidney Systems
• Three slightly overlapping kidney systems are formed in a cranial-to-
caudal sequence
• The pronephros, mesonephros, and metanephros
• The pronephros is rudimentary and non functional; the mesonephros
function for a short time during the early fetal period; the
metanephros forms the permanent kidney.
4. Pronephros
• At the beginning of the fourth week, is represented by 7 to 10 solid
cell groups in the cervical region
• These groups form vestigial excretory units (nephrotomes), that
regress before more caudal ones are formed
• By the end of the fourth week, all indications of the pronephric
system have disappeared.
5. Mesonephros
• The mesonephros and mesonephric ducts are derived from
intermediate mesoderm from upper thoracic to upper lumbar (L3)
segments
• During regression of the pronephric system, the first excretory
tubules of the mesonephros appear
• Form an S-shaped loop, and acquire a tuft of capillaries that will form
a glomerulus at their medial extremity
• Around the glomerulus, the tubules form Bowman’s capsule
6.
7.
8. Mesonephros
• Laterally, the tubule enters the longitudinal collecting duct known as
the mesonephric or wolffian duct
• The mesonephros forms a large ovoid organ on each side of the
midline
• Since the developing gonad is on its medial side, the ridge formed by
both organs is known as the urogenital ridge
• Cranial tubules and glomeruli show degenerative changes, and by the
end of the second month, the majority have disappeared
9. Metanephros: The Definitive Kidney
• The third urinary organ, the metanephros or permanent kidney,
appears in the fifth week
• Its excretory units develop from metanephric mesoderm
• The development of the duct system differs from that of the other
kidney systems.
10.
11.
12. Collecting System
• Collecting ducts of the permanent kidney develop from the ureteric bud
• An outgrowth of the mesonephric duct close to its entrance to the cloaca
• The bud penetrates the metanephric tissue, which is moulded over its
distal end as a cap
• Subsequently, the bud dilates, forming the primitive renal pelvis, and splits
into cranial and caudal portions, the future major calyces
• Each calyx forms two new buds while penetrating the metanephric tissue.
These buds continue to subdivide until 12 or more generations of tubules
have formed
13.
14. Excretory System
• Each newly formed collecting tubule is covered at its distal end by a
metanephric tissue cap
• Under the inductive influence of the tubule, cells of the tissue cap form
small vesicles, which in turn give rise to small S-shaped tubules
• Capillaries grow into the pocket at one end of the S and differentiate into
glomeruli
• These tubules, together with their glomeruli, form nephrons ( excretory
units)
15.
16.
17. Bladder and Urethra
• During the 4th to 7th week the cloaca divides into the urogenital sinus
anterior and the anal canal posterior
• The urorectal septum is a layer of mesoderm btn the primitive anal canal
and the urogenital sinus, The tip of the septum will form the perineal body
• 3 positions of the urogenital sinus can be distinguished: Upper and largest
part (Urinary Bladder)
• The urachus remains attached to the apex of the bladder and the umbilicus
after the allantois is obliterated (Median umbilical ligament)
• Next part is the pelvic part of the urogenital sinus (Prostatic and
membranous parts of the urethra)
• The last part is the phallic part of the urogenital sinus
18.
19. Bladder and Urethra
• The mucosa of the bladder formed by incorporation of the ducts (the
trigone of the bladder) is also mesodermal
• With time, the mesodermal lining of the trigone is replaced by
endodermal epithelium
• At the end of the third month, epithelium of the prostatic urethra
begins to proliferate and forms a number of outgrowths that
penetrate the surrounding mesenchyme(prostate gland, urethral and
paraurethral glands)
20.
21.
22. Genital system
• The key to sexual dimorphism is the Y chromosome, which contains
the testis-determining gene called the SRY (sex-determining region on
Y)
• Its found on the short arm (Yp11)
• The protein product of this gene initiates a cascade of genes that
determine the fate of the rudimentary sexual organs
• In the abscess of the SRY protein the female development is
established
23. Gonads
• The gonads do not acquire male or female morphology
characteristics until the seventh week of development
• Gonads appear initially as a pair of longitudinal ridges (Genital or
Gonadal ridges)
• They are formed by proliferation of the epithelium and a
condensation of underlying mesenchyme
• Germ cells do not appear in the genital ridges until the sixth week of
development
• If they(PGC’s) fail to reach the gonads, the gonads do not develop
• primitive sex cords
24.
25. Testis
• Under influence of the SRY gene on the Y chromosome, which encodes the
testis determining factor,
• The primitive sex cords continue to proliferate and penetrate deep into the
medulla to form the testis or medullary cords
• The cords break up into a network of tiny cell strands that later give rise to
tubules of the rete testis
• During further development, a dense layer of fibrous connective tissue, the
tunica albuginea, separates the testis cords from the surface epithelium
• Testis cords are now composed of primitive germ cells and sustentacular
cells of Sertoli derived from the surface epithelium of the gland
26.
27. Testis
• Interstitial cells of Leydig, derived from the original mesenchyme of
the gonadal ridge, lie between the testis cords.
• By the eighth week of gestation, Leydig cells begin production of
testosterone and the testis is able to influence sexual differentiation
of the genital ducts and external genitalia
• Testis cords remain solid until puberty, when they acquire a lumen,
thus forming the seminiferous tubules, they join the rete testis
tubules, which in turn enter the ductuli efferences
• They link the rete testis and the mesonephric or wolffian duct, which
becomes the ductus deferens
28.
29. Ovary
• No Y chromosome, primitive sex cords dissociate into irregular cell
clusters
• Later, they disappear and are replaced by a vascular stroma that
forms the ovarian medulla
• The surface epithelium of the female gonad, unlike that of the male,
continues to proliferate
• In the seventh week, it gives rise to a second generation of cords,
cortical cords, which penetrate the underlying mesenchyme but
remain close to the surface
• Cell clusters form Follicular cells (Primordial follicle)
30.
31. Genital Ducts
• The paramesonephric duct arises as a longitudinal invagination of the
epithelium on the anterolateral surface of the urogenital ridge
Cranially, the duct opens into the abdominal cavity with a funnel-like
structure
• Caudally, it first runs lateral to the mesonephric duct, then crosses it
ventrally to grow caudomedially
• The two ducts are initially separated by a septum but later fuse to form the
uterine canal
• The combined ducts projects into the posterior wall of the urogenital sinus,
where it causes a small swelling, the paramesonephric or müllerian
tubercle
32.
33.
34.
35.
36.
37.
38. External genitalia
• In the third week , mesenchyme cells originating from the primitive streak
migrate around the cloacal membrane to form cloacal folds
• Cranial to the cloacal membrane the folds unite to form the genital
tubercle
• Caudally the are subdivided into urethral folds anteriorly and anal folds
posteriorly
• Another pair of elevations, the genital swellings become visible on each
side of the urethral folds, they later from scrotum or labia majora
• At the end of the sixth week it is still impossible to distinguish between the
two sexes
39.
40. External Genitalia in the Male
• Influence of androgens secreted by the fetal testes
• Characterized by rapid elongation of the genital tubercle, which is now
called the phallus
• During this elongation, the phallus pulls the urethral folds forward so that
they form the lateral walls of the urethral groove
• The epithelial lining of the groove (Endoderm) forms the urethral plate
• At the end of the 3rd month the two urethral folds close over the urethral
plate, forming a penile urethra, does not extend to the tip of the phallus
• Scrotal swellings/genital swellings arise from the inguinal region, move
medially were they are only separated by the scrotal septum
41.
42. External Female Genitalia
• Under the influence of estrogens
• The genital tubercle elongates only slightly (Clitoris), but it is larger
than in males during the early stages of development(3rd and 4th
month)
• Urethral folds do not fuse (Labia minora)
• Genital swellings enlarge (Labia majora)
• The open urogenital groove forms the vestibule
43.
44. Descent of the Testes
• Toward the end of the second month, the urogenital mesentery attaches the
testis and mesonephros to the posterior abdominal wall
• The mesonephros degenerates to form a mesentery for the Gonad
• Caudally it becomes the caudal genital ligament
• Also extending from the caudal pole of the testis is condensed mesenchymal
tissue (Gubernaculum), which terminates in the inguinal region
• As the testis begin to descend the towards the internal ring , an extra-abdominal
portion forms, from the inguinal region to the scrotal swellings
• Factors causing descent are unclear but could be increased intra abdominal
pressure, Hormones (androgens and MIS)
• Testis are at the inguinal region around 12 weeks and reach the scrotum by
33weeks
In the male, a few of the caudal tubules and the mesonephric duct persist and participate in formation of the genital system, but they disappear in the female.
The ureteric bud gives rise to the ureter, the renal pelvis, the major and minor calyces, and approximately 1 to 3 million collecting tubules.
The distal end forms an open connection with one of the collecting tubules, establishing a passageway from Bowman’s capsule to the collecting unit
Continuous lengthening of the excretory tubule results in formation of the proximal convoluted tubule, loop of Henle, and distal convoluted tubule
Nephrons are formed until birth, at which time there are approximately 1 million in each kidney.
Urine production begins early in gestation, soon after differentiation of the glomerular capillaries, which start to form by the 10th week
During differentiation of the cloaca, the caudal portions of the mesonephric ducts are absorbed into the wall of the urinary bladder
those of the mesonephric ducts move close together to enter the prostatic urethra and in the male become the ejaculatory ducts
Hence, the primordial germ cells have an inductive infl uence on development of the gonad into ovary or testis
These efferent ductules are the remaining parts of the excretory tubules of the mesonephric system
In embryos with an XX sex chromosome confi guration, medullary cords of the gonad regress, and a secondary generation of cortical cords develops
The mesonephric ducts open into the urogenital sinus on either side of the müllerian tubercle.
The paramesonephric ducts develop into the main genital ducts of the female
Initially, three parts can be recognized in each duct: (1) a cranial vertical portion that opens into the abdominal cavity, (2) a horizontal part that crosses the mesonephric duct, and (3) a caudal vertical part that fuses with its partner from the opposite side
With descent of the ovary, the first two parts develop into the uterine tube and the caudal parts fuse to form the uterine canal.
After the ducts fuse in the midline, a broad transverse pelvic fold is established, the broad ligament of the uterus
As the mesonephros regresses, a few excretory tubules, the epigenital tubules, establish contact with cords of the rete testis and finally form the efferent ductules of the testis
Immediately below the entrance of the efferent ductules, the mesonephric ducts elongate and become highly convoluted, forming the (ductus) epididymis
From the tail of the epididymis to the outbudding of the seminal vesicle, the mesonephric ducts obtain a thick muscular coat and form the ductus deferens.
Shortly after the solid tip of the paramesonephric ducts reaches the urogenital sinus
2 solid evaginations grow out from the pelvic part of the sinus sinovaginal bulbs, proliferate and form a solid vaginal plate.
Proliferation continues at the cranial end of the plate, increasing the distance between the uterus and the urogenital sinus
By the fifth month, the vaginal outgrowth is entirely canalized
The wing-like expansions of the vagina around the end of the uterus, the vaginal fornices, are of paramesonephric origin
The lumen of the vagina remains separated from that of the urogenital sinus by a thin tissue plate, the hymen
Most distal urethra forms during the 4th month , when ectodermal cells from the tip of the glans penetrate inward and form a short epithelial cord, which later forms the external urethral meatus
Blood supply from the aorta is retained
Hence, the processus vaginalis, accompanied by the muscular and fascial layers of the body wall, evaginates into the scrotal swelling, forming the inguinal canal