Gb turner syndrome
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Turner Syndrome is a genetic condition that affects development in females and is caused by the absence of one X chromosome. The effects at birth can include swollen hands, feet, and face. While there is no prevention or cure, doctors can test for it at birth through a karyotype and monitor development. Those with Turner Syndrome are typically shorter in height and may struggle with fertility.
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Resli W. - Living with Turner Syndrome
Turner syndrome is a genetic condition that affects girls where one of the two X chromosomes is missing or partially missing. It occurs in around 1 in 2,500 live female births. Girls with Turner syndrome are shorter in height and may experience a variety of health issues such as heart problems, kidney problems, low set ears, skin moles, and celiac disease. However, with growth hormone treatment and medical care, girls can live healthy lives and are otherwise similar to their peers.
Turner syndrome (1)
Turner syndrome is a genetic condition that affects development in females caused by partial or complete absence of the second X chromosome. It was first discovered in 1938 and named after Dr. Henry Turner. Common symptoms include short stature, lack of sexual maturation, infertility, and cardiovascular issues. It is diagnosed through a karyotype blood test that shows a monosomy, or missing chromosome. While there is no cure, treatment can help manage certain medical conditions. It occurs in around 1 in 2,500 live female births.
Turner syndrome
Turner syndrome is a genetic condition that affects 1 in 2,500 girls and is caused by a missing or partial X chromosome. Girls with Turner syndrome are usually short and have delayed sexual development due to ovarian issues. They may experience other health problems as well, including heart and kidney issues. While there is no cure, growth hormone treatment can help increase height and estrogen therapy can induce puberty. With medical care and support, people with Turner syndrome can lead healthy lives.
Turner syndrome
Turner's syndrome is a genetic disorder where females are born with a missing or partial X chromosome. It can cause various health issues like heart defects, high blood pressure, and delayed puberty. A karyotype test is used to diagnose it, which identifies if an X chromosome is missing. While there is no prevention, treatment focuses on hormone replacement and managing health complications.
Turner syndrome presentation last
Turner syndrome is caused by complete or partial monosomy of the X chromosome in females. It is characterized by short stature, infertility, and other physical traits. The document discusses the history and genetics of Turner syndrome, including that the most common karyotype is 45,X and variants involve an isochromosome or ring chromosome. Phenotypic features can range from mild to severe and include lymphedema, heart and kidney problems, learning disabilities, and infertility. Prenatal diagnoses are now possible by ultrasound abnormalities or amniocentesis. Treatment focuses on growth hormone, estrogen therapy, and managing associated health issues.
Gh therapy turner syndrome by swathi lakshmi
Growth hormone therapy is an important part of managing Turner syndrome. It increases growth velocity and leads to modest increases in adult height. The optimal age to start growth hormone treatment is at least 4 years before puberty. While growth hormone therapy is generally safe, risks can include intracranial hypertension and slipped capital femoral epiphysis. Clinical evidence shows that growth hormone therapy in young girls with Turner syndrome increases height standard deviation scores by about 1 standard deviation over 2 years. It also promotes linear growth and increases bone mass and metabolism.
Turnerâs syndrome
Turner's syndrome is a genetic condition that affects development in females caused by a missing or partial X chromosome. Common symptoms include short stature, broad chest, increased weight, and reproductive sterility. While there is no cure, treatment options focus on hormone therapy to promote growth and reduce osteoporosis risks, as well as modern reproductive technologies. Turner's syndrome is usually inherited from the father and patients can live normal lives with close medical monitoring.
Turners Syndrome
Turner syndrome is a genetic condition that affects development in girls caused by a missing or partial X chromosome. It was first described in 1938 by Dr. Henry Turner. Common characteristics include short stature, ovarian dysfunction leading to infertility, and heart defects. Diagnosis involves chromosome analysis from amniocentesis or blood tests. Treatment may include growth hormone, estrogen therapy, and assisted reproduction. Research continues on treatments and managing associated health problems throughout life.
Recommended
Resli W. - Living with Turner Syndrome
Turner syndrome is a genetic condition that affects girls where one of the two X chromosomes is missing or partially missing. It occurs in around 1 in 2,500 live female births. Girls with Turner syndrome are shorter in height and may experience a variety of health issues such as heart problems, kidney problems, low set ears, skin moles, and celiac disease. However, with growth hormone treatment and medical care, girls can live healthy lives and are otherwise similar to their peers.
Turner syndrome (1)
Turner syndrome is a genetic condition that affects development in females caused by partial or complete absence of the second X chromosome. It was first discovered in 1938 and named after Dr. Henry Turner. Common symptoms include short stature, lack of sexual maturation, infertility, and cardiovascular issues. It is diagnosed through a karyotype blood test that shows a monosomy, or missing chromosome. While there is no cure, treatment can help manage certain medical conditions. It occurs in around 1 in 2,500 live female births.
Turner syndrome
Turner syndrome is a genetic condition that affects 1 in 2,500 girls and is caused by a missing or partial X chromosome. Girls with Turner syndrome are usually short and have delayed sexual development due to ovarian issues. They may experience other health problems as well, including heart and kidney issues. While there is no cure, growth hormone treatment can help increase height and estrogen therapy can induce puberty. With medical care and support, people with Turner syndrome can lead healthy lives.
Turner syndrome
Turner's syndrome is a genetic disorder where females are born with a missing or partial X chromosome. It can cause various health issues like heart defects, high blood pressure, and delayed puberty. A karyotype test is used to diagnose it, which identifies if an X chromosome is missing. While there is no prevention, treatment focuses on hormone replacement and managing health complications.
Turner syndrome presentation last
Turner syndrome is caused by complete or partial monosomy of the X chromosome in females. It is characterized by short stature, infertility, and other physical traits. The document discusses the history and genetics of Turner syndrome, including that the most common karyotype is 45,X and variants involve an isochromosome or ring chromosome. Phenotypic features can range from mild to severe and include lymphedema, heart and kidney problems, learning disabilities, and infertility. Prenatal diagnoses are now possible by ultrasound abnormalities or amniocentesis. Treatment focuses on growth hormone, estrogen therapy, and managing associated health issues.
Gh therapy turner syndrome by swathi lakshmi
Growth hormone therapy is an important part of managing Turner syndrome. It increases growth velocity and leads to modest increases in adult height. The optimal age to start growth hormone treatment is at least 4 years before puberty. While growth hormone therapy is generally safe, risks can include intracranial hypertension and slipped capital femoral epiphysis. Clinical evidence shows that growth hormone therapy in young girls with Turner syndrome increases height standard deviation scores by about 1 standard deviation over 2 years. It also promotes linear growth and increases bone mass and metabolism.
Turnerâs syndrome
Turner's syndrome is a genetic condition that affects development in females caused by a missing or partial X chromosome. Common symptoms include short stature, broad chest, increased weight, and reproductive sterility. While there is no cure, treatment options focus on hormone therapy to promote growth and reduce osteoporosis risks, as well as modern reproductive technologies. Turner's syndrome is usually inherited from the father and patients can live normal lives with close medical monitoring.
Turners Syndrome
Turner syndrome is a genetic condition that affects development in girls caused by a missing or partial X chromosome. It was first described in 1938 by Dr. Henry Turner. Common characteristics include short stature, ovarian dysfunction leading to infertility, and heart defects. Diagnosis involves chromosome analysis from amniocentesis or blood tests. Treatment may include growth hormone, estrogen therapy, and assisted reproduction. Research continues on treatments and managing associated health problems throughout life.
Conditions: Turner Syndrome Chrom
Turner syndrome is a genetic condition that affects development in females who are missing an entire X chromosome or part of an X chromosome. Some key features of Turner syndrome include short stature, infertility, and certain physical traits like puffy hands and feet. Antenatal findings may include cystic hygroma and neonatal features can include lymphedema and heart defects. Karyotypes of patients with Turner syndrome often show a single X chromosome (45,X) or mosaicism. Treatment options focus on hormone replacement and growth therapy to improve development and quality of life.
Turner Syndrome
Turner syndrome is a chromosomal condition that affects female development. It occurs when one of the two X chromosomes is missing or incomplete in girls, resulting in short stature, infertility, and other physical signs. Treatment focuses on growth hormone therapy, estrogen replacement, managing heart and hearing issues, and monitoring for high blood pressure, thyroid problems, and diabetes. While women with Turner syndrome are typically infertile, pregnancy may potentially be possible with donor embryos and medical support.
Turner syndrome
Turner Syndrome is a chromosomal condition that affects females and occurs in about 1 in 2,500 births. It is caused by a full or partial missing of the second X chromosome, resulting in a karyotype of 45,XO. Clinical features include short stature, lack of sexual development at puberty, and other health issues. Diagnosis can be made at birth based on symptoms or later in life if a person does not grow or develop normally. Treatment involves growth hormone injections, estrogen replacement therapy, and monitoring for conditions like heart problems, ear infections, and high blood pressure.
Turner’s Syndrome Project
Turner's syndrome is a genetic condition that affects females and is caused by partial or complete absence of one of the X chromosomes. It occurs in about 1 in 2,500 live female births. Common symptoms include short stature, underdeveloped or absent sexual organs, swollen hands and feet, eye problems, and heart issues. While Turner's syndrome cannot be cured, treatment focuses on hormone replacement, surgery, and lifestyle management to address symptoms and health complications.
Turner's Syndrome
Turner syndrome (gonadal dysgenesis) is one of the most common chromosomal abnormalities occuring 1 in 2500 to 1 in 3000 live-born girls. It is an important cause of short stature in girls and primary amenorrhea in young women that is usually caused by loss of part or all of an X chromosome. This review briefly summarises the current knowledge about the syndrome and the management strategies.
Turner syndrome
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A Case Analysis of Turner’s syndrome for Neonate_Crimson Publishers
An 8-day old female infant was admitted to the hospital for shortness of breath. She displayed several physical features characteristic of Turner's syndrome including short stature, edema in the lower legs and neck, and poorly developed toenails. Laboratory tests found a low sex hormone level and chromosomal analysis revealed a 45,XO karyotype, consistent with Turner's syndrome. She was diagnosed with Turner's syndrome, pneumonia, and a heart condition. Her condition improved with treatment but she was discharged upon her parents' request before being fully recovered.
Pervasive developmental disorders (turner syndrome, klinefelter's syndrome)
Turner syndrome is a genetic condition that affects females, caused by missing or abnormal X chromosome. It can cause short stature, lack of sexual development at puberty, infertility, and other issues. Klinefelter syndrome is a condition in males caused by an extra X chromosome, resulting in enlarged breasts and reduced facial/body hair. Fragile X syndrome is caused by a gene on the X chromosome shutting down, leading to intellectual disabilities, large ears, joint issues, and other traits.
Turner syndrome
Turner syndrome is a genetic condition where a female is missing an X chromosome. It was discovered by Henry Turner in 1938. Common symptoms include short stature, swollen hands and feet at birth, and issues developing menstrual periods and breasts without hormone treatment. Those with Turner syndrome also often have heart defects, diabetes, and vision or hearing problems. While there is no cure, treatment can help increase height and promote breast and hip development. Turner syndrome occurs in about 1 in 2000 to 1 in 5000 females and is usually not inherited from parents.
Turner's syndrome
Turner syndrome is a genetic condition where females are missing an X chromosome. It affects about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. While it cannot be passed down from parent to child, it is typically caused by a failure of chromosomes to separate during egg formation. Diagnosis is often made based on physical characteristics, and can be confirmed with a blood test. Hormone replacement therapy is the primary treatment.
Turners syndrome
Turner syndrome is a genetic condition that affects development in females caused by a full or partial missing X chromosome. It occurs in about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. Treatment involves hormone replacement therapy including growth hormone, androgens, and estrogen to promote normal development and replace missing hormones.
Turner syndrome
Turner syndrome
Prevalence, Types of chromosomal anomalies, Typical Features, Diagnosis, Monitoring, Management, Adult Management
TURNER SYNDROME
45X LOSS OF WHOLE OR PART OF X XP DELETION OR XQ DELETION OR ISO CHROMOSOME XP OR XQ OR RING CHROMOSOME X
CLINICAL FEATURES- FEMALE INFANTILISM
• Webbed neck * Coarctation and other cardiac AS A R
• Short height * Horseshoe kidney
• Broad chest * Hypothyroidism
• Wide carrying angle arm * High LH FSH
• Infantile ovaries
Turner syndrome
Turner syndrome is a genetic condition characterized by complete or partial monosomy of the X chromosome, affecting about 1 in 2,500-5,000 females. Clinical features include short stature, neck webbing, protruding ears, and gonadal dysgenesis leading to infertility. It is diagnosed through karyotyping and fetal ultrasound may suggest it. Treatment involves growth hormone therapy, estrogen replacement, and managing associated conditions such as hypothyroidism, diabetes, and heart problems. Prognosis is generally good with treatment, though individuals are often shorter and infertile.
Klinefelter Syndrome
Klinefelter syndrome is a genetic disorder that affects males, occurring when a boy is born with one or more extra X chromosomes. It affects about 1 in 1000 males. The condition was first identified in 1942 and involves small testes, infertility and other issues. Diagnosis involves hormone testing and chromosome analysis showing 47,XXY karyotype in most cases. Symptoms may include language delays, tall stature, and breast development at puberty. Treatment focuses on testosterone therapy, fertility options, and addressing physical and psychological issues.
Trisomy 8, Turners syndrome, Triple X: A Case Report
This case report describes a 13-year-old female patient with three rare genetic conditions: Trisomy 8, Turner Syndrome, and Triple X Syndrome. She presented with refractive errors, oculomotor dysfunction, and impaired vision information processing. After 27 optometric vision therapy sessions targeting these issues, her visual skills improved to age-appropriate levels. This is the first reported case of a patient with all three syndromes, demonstrating that vision therapy can effectively treat visual problems in individuals with genetic anomalies.
Klinefelter syndrome
Klinefelter syndrome is a genetic condition that affects males, causing reduced fertility, weaker muscles, and other symptoms. It results from an extra X chromosome. As babies and children, those with Klinefelter syndrome may be less confident and active than other boys. As adults, they can live normal lives. Treatment may include testosterone therapy, surgery to reduce breast size, and addressing infertility issues.
Klinefeltersyndrome 120322141345-phpapp02
Klinefelter syndrome is a genetic condition caused by the presence of an extra X chromosome, resulting in a 47, XXY chromosome pattern. It is one of the most common sex chromosome abnormalities in males. Individuals with Klinefelter syndrome are typically infertile and experience learning disabilities as well as physical symptoms like enlarged breasts and sparse body hair. The condition is diagnosed through a karyotype analysis and treated with testosterone therapy to promote normal development.
Klinefelter’s Syndrome
07-08-2013
Faculty of medicine of Syrian Private University.
Please LIKE my page! http://facebook.com/NawrasAlHalabi
متلازمة كلاينفلتر وتقانات أطفال الأنابيب
.كلية الطب البشري في الجامعة السورية الخاصة
Turner's syndrome
Turner syndrome is a genetic condition where females are missing an entire or partial X chromosome. It affects about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. While it cannot be passed down from parent to child, it is typically caused during egg formation when chromosomes fail to separate properly. Diagnosis involves a karyotype blood test and treatment focuses on hormone replacement therapy to promote normal development and replace missing hormones.
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Conditions: Turner Syndrome Chrom
Turner syndrome is a genetic condition that affects development in females who are missing an entire X chromosome or part of an X chromosome. Some key features of Turner syndrome include short stature, infertility, and certain physical traits like puffy hands and feet. Antenatal findings may include cystic hygroma and neonatal features can include lymphedema and heart defects. Karyotypes of patients with Turner syndrome often show a single X chromosome (45,X) or mosaicism. Treatment options focus on hormone replacement and growth therapy to improve development and quality of life.
Turner Syndrome
Turner syndrome is a chromosomal condition that affects female development. It occurs when one of the two X chromosomes is missing or incomplete in girls, resulting in short stature, infertility, and other physical signs. Treatment focuses on growth hormone therapy, estrogen replacement, managing heart and hearing issues, and monitoring for high blood pressure, thyroid problems, and diabetes. While women with Turner syndrome are typically infertile, pregnancy may potentially be possible with donor embryos and medical support.
Turner syndrome
Turner Syndrome is a chromosomal condition that affects females and occurs in about 1 in 2,500 births. It is caused by a full or partial missing of the second X chromosome, resulting in a karyotype of 45,XO. Clinical features include short stature, lack of sexual development at puberty, and other health issues. Diagnosis can be made at birth based on symptoms or later in life if a person does not grow or develop normally. Treatment involves growth hormone injections, estrogen replacement therapy, and monitoring for conditions like heart problems, ear infections, and high blood pressure.
Turner’s Syndrome Project
Turner's syndrome is a genetic condition that affects females and is caused by partial or complete absence of one of the X chromosomes. It occurs in about 1 in 2,500 live female births. Common symptoms include short stature, underdeveloped or absent sexual organs, swollen hands and feet, eye problems, and heart issues. While Turner's syndrome cannot be cured, treatment focuses on hormone replacement, surgery, and lifestyle management to address symptoms and health complications.
Turner's Syndrome
Turner syndrome (gonadal dysgenesis) is one of the most common chromosomal abnormalities occuring 1 in 2500 to 1 in 3000 live-born girls. It is an important cause of short stature in girls and primary amenorrhea in young women that is usually caused by loss of part or all of an X chromosome. This review briefly summarises the current knowledge about the syndrome and the management strategies.
Turner syndrome
If my presentation was useful for you, you maybe could support me with some donation. Thanks
Paypal: mostafabkh
A Case Analysis of Turner’s syndrome for Neonate_Crimson Publishers
An 8-day old female infant was admitted to the hospital for shortness of breath. She displayed several physical features characteristic of Turner's syndrome including short stature, edema in the lower legs and neck, and poorly developed toenails. Laboratory tests found a low sex hormone level and chromosomal analysis revealed a 45,XO karyotype, consistent with Turner's syndrome. She was diagnosed with Turner's syndrome, pneumonia, and a heart condition. Her condition improved with treatment but she was discharged upon her parents' request before being fully recovered.
Pervasive developmental disorders (turner syndrome, klinefelter's syndrome)
Turner syndrome is a genetic condition that affects females, caused by missing or abnormal X chromosome. It can cause short stature, lack of sexual development at puberty, infertility, and other issues. Klinefelter syndrome is a condition in males caused by an extra X chromosome, resulting in enlarged breasts and reduced facial/body hair. Fragile X syndrome is caused by a gene on the X chromosome shutting down, leading to intellectual disabilities, large ears, joint issues, and other traits.
Turner syndrome
Turner syndrome is a genetic condition where a female is missing an X chromosome. It was discovered by Henry Turner in 1938. Common symptoms include short stature, swollen hands and feet at birth, and issues developing menstrual periods and breasts without hormone treatment. Those with Turner syndrome also often have heart defects, diabetes, and vision or hearing problems. While there is no cure, treatment can help increase height and promote breast and hip development. Turner syndrome occurs in about 1 in 2000 to 1 in 5000 females and is usually not inherited from parents.
Turner's syndrome
Turner syndrome is a genetic condition where females are missing an X chromosome. It affects about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. While it cannot be passed down from parent to child, it is typically caused by a failure of chromosomes to separate during egg formation. Diagnosis is often made based on physical characteristics, and can be confirmed with a blood test. Hormone replacement therapy is the primary treatment.
Turners syndrome
Turner syndrome is a genetic condition that affects development in females caused by a full or partial missing X chromosome. It occurs in about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. Treatment involves hormone replacement therapy including growth hormone, androgens, and estrogen to promote normal development and replace missing hormones.
Turner syndrome
Turner syndrome
Prevalence, Types of chromosomal anomalies, Typical Features, Diagnosis, Monitoring, Management, Adult Management
TURNER SYNDROME
45X LOSS OF WHOLE OR PART OF X XP DELETION OR XQ DELETION OR ISO CHROMOSOME XP OR XQ OR RING CHROMOSOME X
CLINICAL FEATURES- FEMALE INFANTILISM
• Webbed neck * Coarctation and other cardiac AS A R
• Short height * Horseshoe kidney
• Broad chest * Hypothyroidism
• Wide carrying angle arm * High LH FSH
• Infantile ovaries
Turner syndrome
Turner syndrome is a genetic condition characterized by complete or partial monosomy of the X chromosome, affecting about 1 in 2,500-5,000 females. Clinical features include short stature, neck webbing, protruding ears, and gonadal dysgenesis leading to infertility. It is diagnosed through karyotyping and fetal ultrasound may suggest it. Treatment involves growth hormone therapy, estrogen replacement, and managing associated conditions such as hypothyroidism, diabetes, and heart problems. Prognosis is generally good with treatment, though individuals are often shorter and infertile.
Klinefelter Syndrome
Klinefelter syndrome is a genetic disorder that affects males, occurring when a boy is born with one or more extra X chromosomes. It affects about 1 in 1000 males. The condition was first identified in 1942 and involves small testes, infertility and other issues. Diagnosis involves hormone testing and chromosome analysis showing 47,XXY karyotype in most cases. Symptoms may include language delays, tall stature, and breast development at puberty. Treatment focuses on testosterone therapy, fertility options, and addressing physical and psychological issues.
Trisomy 8, Turners syndrome, Triple X: A Case Report
This case report describes a 13-year-old female patient with three rare genetic conditions: Trisomy 8, Turner Syndrome, and Triple X Syndrome. She presented with refractive errors, oculomotor dysfunction, and impaired vision information processing. After 27 optometric vision therapy sessions targeting these issues, her visual skills improved to age-appropriate levels. This is the first reported case of a patient with all three syndromes, demonstrating that vision therapy can effectively treat visual problems in individuals with genetic anomalies.
Klinefelter syndrome
Klinefelter syndrome is a genetic condition that affects males, causing reduced fertility, weaker muscles, and other symptoms. It results from an extra X chromosome. As babies and children, those with Klinefelter syndrome may be less confident and active than other boys. As adults, they can live normal lives. Treatment may include testosterone therapy, surgery to reduce breast size, and addressing infertility issues.
Klinefeltersyndrome 120322141345-phpapp02
Klinefelter syndrome is a genetic condition caused by the presence of an extra X chromosome, resulting in a 47, XXY chromosome pattern. It is one of the most common sex chromosome abnormalities in males. Individuals with Klinefelter syndrome are typically infertile and experience learning disabilities as well as physical symptoms like enlarged breasts and sparse body hair. The condition is diagnosed through a karyotype analysis and treated with testosterone therapy to promote normal development.
Klinefelter’s Syndrome
07-08-2013
Faculty of medicine of Syrian Private University.
Please LIKE my page! http://facebook.com/NawrasAlHalabi
متلازمة كلاينفلتر وتقانات أطفال الأنابيب
.كلية الطب البشري في الجامعة السورية الخاصة
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A Case Analysis of Turner’s syndrome for Neonate_Crimson Publishers
A Case Analysis of Turner’s syndrome for Neonate_Crimson Publishers
Pervasive developmental disorders (turner syndrome, klinefelter's syndrome)
Pervasive developmental disorders (turner syndrome, klinefelter's syndrome)
Trisomy 8, Turners syndrome, Triple X: A Case Report
Trisomy 8, Turners syndrome, Triple X: A Case Report
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Turner's syndrome
Turner syndrome is a genetic condition where females are missing an entire or partial X chromosome. It affects about 1 in 2,500 baby girls. Common characteristics include short stature and lack of ovarian development leading to infertility. While it cannot be passed down from parent to child, it is typically caused during egg formation when chromosomes fail to separate properly. Diagnosis involves a karyotype blood test and treatment focuses on hormone replacement therapy to promote normal development and replace missing hormones.
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Turner's Syndrome_.pdf
The document discusses Turner syndrome, a genetic condition where a female is born with only one X chromosome instead of the typical two. It provides background on the syndrome's discovery and symptoms to expect. Common symptoms include short stature, heart issues, infertility, and learning disabilities. Treatment focuses on growth hormone therapy, estrogen therapy, and psychological support to address medical, developmental, and social difficulties associated with Turner syndrome.
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TURNER’S SYNDROME.pptx
Turner syndrome (TS), sometimes referred to as congenital ovarian hypoplasia syndrome is a chromosomal disorder that is the most common sex chromosomal abnormality affecting girls and women.
It occurs in about 1 out of every 5000 live female births and affects all races and regions of the world equally. Turner syndrome is a genetic disorder, but it’s usually not inherited, except in very rare cases.
The name "Turner’s syndrome" comes from Dr. Henry Turner, the physician who first described the collection of its findings in 1938. However, it was not until 1959 that the cause of Turner syndrome was identified. This is the presentation on it.
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genetic disoeders.ppt
1. Down syndrome is caused by trisomy 21 and is characterized by intellectual disability and distinctive physical features. It is the most common genetic chromosomal disorder.
2. Turner syndrome is caused by a missing or partial X chromosome and affects growth and sexual development in females, causing short stature and infertility.
3. Klinefelter syndrome is the most common sex chromosome disorder in males, caused by at least one extra X chromosome, and is associated with infertility and less developed secondary sex characteristics.
Brain
Turner syndrome is a chromosomal condition that affects development in girls. It results from missing or partial X chromosome, so girls with Turner syndrome have only one X chromosome instead of the typical two. Signs and symptoms include short stature, low-set ears, extra folds of skin on the neck, and irregular or absent menstrual periods. Health issues associated with Turner syndrome include heart defects, kidney problems, diabetes, and hearing loss. Diagnosis is made through a chromosomal test called a karyotype that shows the missing or partial chromosome. Treatment focuses on hormone therapy, cardiac surgery if needed, and reproductive technologies to help with pregnancy.
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82085243 case-study-on-pregnancy-induced-hypertension-eclampsia
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DO YOU KNOW WHICH “HERNIA” YOU ARE SUFFERING FROM?
DO YOU KNOW WHICH “HERNIA” YOU ARE SUFFERING FROM?
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8th Science Slide
God created all matter and the elements. He arranged them in an orderly pattern, like the Periodic Table, and gave each unique properties. God also gave us energy and the ability to understand forces and motion. Jesus is the light that guides us, just as light guides our understanding of the physical world. Throughout science, we can see God's design and fingerprints on his creation.
8th grade science bible integration
This document provides a summary of 8th grade science concepts with biblical integration. It covers topics like matter, atoms and the periodic table, chemical bonds, chemical reactions, acids and bases, energy, thermal energy, motion, forces, electricity, sound, and light. For each topic, it lists 3-4 key points and relates them to a bible verse, with the overarching message that God created an orderly system and wants Christians to use their understanding of it to better know and serve him.
8th Grade Science Review Bible Integration
God created all things, including matter and energy. The document provides a summary of key concepts from 8th grade science, with biblical verses integrated throughout. It covers topics like the states of matter, atoms and the periodic table, chemical bonds and reactions, acids and bases, forms of energy, motion, forces, magnetism, electricity, sound, and light. The summaries highlight that all things were made by God and that science reveals aspects of his creation and power.
Jordan biblical Integration
This document provides a summary of 8th grade science topics from a biblical perspective. Each topic includes 1-3 bible verses that relate to the science concepts and 3-5 bullet points summarizing the key ideas. The topics covered include matter, atoms and the periodic table, chemical bonds, chemical reactions, acids and bases, energy, thermal energy, motion, forces, magnetism, electricity, sound, and light.
8th larry
This document provides a summary of key science concepts related to matter, atoms, chemical bonds, reactions, acids and bases, energy, motion, forces, magnetism, electricity, sound, and light. Each section includes a Bible verse and brief explanation of how it relates to the science topic. The concepts are defined concisely, such as the three states of matter, atomic structure, types of chemical bonds and energy, forms of motion, types of forces, properties of magnets and electricity, characteristics of sound and light waves.
8th grade science jb
This document contains a summary of key concepts from an 8th grade science textbook organized by topic. The topics covered include matter, atoms and the periodic table, chemical bonds, chemical reactions, acids and bases, energy, thermal energy, motion, forces, magnetism, electricity, sound, and light. For each topic, there is a brief 1-2 sentence definition or description of the science concept and it is related to a Bible verse.
Fireworks Michael and Matthew
The document describes the anatomy, history, and chemistry of fireworks. It explains that fireworks work by using black powder to launch shells into the air, where a secondary fuse then ignites stars that explode and produce colorful patterns. Fireworks were invented in China by monks mixing saltpeter, sulfur, and charcoal to produce the first rockets. The document provides safety tips and lists different chemical elements that burn specific colors when used in fireworks.
Fire works from ben
Fireworks contain black powder, fuses, and colored elements that produce different colors when burned. Chemical reactions occur when compounds are mixed with black powder to create stars of different colors - yellow comes from sodium, orange from calcium, red from strontium, green from barium, and blue or purple from copper or strontium. Fireworks were invented in China over 1,000 years ago using black powder made from saltpeter, sulfur, and charcoal. They have since been used in celebrations and displays around the world. Safety tips recommend wearing ear protection and keeping a safe distance from fireworks.
Fireworks s.a.j
This document discusses the history, components, chemistry, and safety of fireworks. It explains that fireworks produce color through the combustion of different metal elements and compounds. Lithium makes red, sodium makes gold and yellow, and barium makes green. The history section notes that the Chinese used black powder over 1000 years ago and that fireworks were used against Mongol invaders in 1279. The document provides safety tips, advising leaving fireworks to professionals and taking reasonable precautions to avoid injuries.
Fireworks Kristin Rj
Fireworks contain a shell, fuse, gunpowder, and stars made of chemicals that produce different colors when burned. Stars are made by mixing chemicals with paste and forming them into balls. The fuse ignites the gunpowder, which explodes and sends the stars into the sky. Common chemicals that make colors include copper for blue, barium for green, and lithium or strontium for red. Fireworks were first invented in China using gunpowder and have been used for entertainment for centuries. Safety tips recommend keeping a distance from fireworks and not approaching any that have not ignited.
Fireworks amn
The document discusses the parts, chemical reactions, and history of fireworks. It describes the main components of fireworks like the black powder fuse, bursting charge, and break. The chemical reaction involves adding raw materials, igniting an energy source to start the reaction, and using the fuse to light the black powder and cause the firework to explode. Different chemical compounds produce different colors when burned. The history section notes that fireworks originated in China and were brought to Italy by Marco Polo. Safety tips recommend having a designated shooter, only using fireworks outdoors, and being prepared with water and safety glasses.
fireworks Imani Josh
Fireworks contain various chemical compounds that produce different colors when burned. Parts of a firework include a break, time delay fuse, and stars that explode separately. A firework is propelled into the air by a lift charge after the fuse ignites black powder in the launching tube. Chemical reactions between substances like potassium chlorate and gunpowder produce heat and light. Common firework designs include palms, chrysanthemums, and roundels. The Chinese invented fireworks over 1000 years ago to scare spirits, and they have since evolved with many technological and safety improvements.
Klinefelter Syndrome HRB.
Kline Felter Syndrome is a genetic disorder where males are born with an extra X chromosome, resulting in XXY sex chromosomes. It occurs due to a random error in the mother and father's sex cells when the baby is conceived. Signs include a taller and less muscular body type, broader hips, larger breasts, weaker bones, and smaller genitals. It can cause learning problems and issues with sexual development or infertility. While there is no cure, treatments can help address symptoms.
Muscular dystrophy ld
Muscular dystrophy is a genetic disorder that causes progressive weakening and loss of muscle mass. It affects muscles that help the body move and can also impact posture and breathing. The disorder is caused by missing or incorrect information in genes or a damaged X chromosome. While there is no cure for muscular dystrophy, treatments like therapy and surgery can help reduce pain. DNA testing allows people to be prepared, but the condition cannot be prevented.
Down's syndrome lm
Down's Syndrome is a genetic disorder caused by the presence of an extra chromosome 21, known as trisomy 21. It is characterized by physical effects like upward slanted eyes, a flat nose, a small head, and short stubby hands. Individuals with Down's Syndrome are also more likely to have heart defects and lung infections. Treatments include medication, surgery to correct issues, proper education and care, and speech or physical therapy. Diagnosis is suggested for mothers over 35 and can be confirmed through blood tests, ultrasounds, or by checking chromosomes.
Gb turner syndrome
Turner Syndrome is a genetic condition that affects development in females and is caused by the absence of one X chromosome. The effects at birth can include swollen hands, feet, and face. While there is no prevention or cure, doctors can test for it at birth through a karyotype and monitor development. Those with Turner Syndrome are typically shorter in height and may struggle with fertility, though pregnancy is possible with medical intervention.
Optic atrophy sa
Optic atrophy is caused by mutations in the OPA1 gene and is inherited in an autosomal dominant pattern. It causes progressive vision loss that typically begins in the first decade of life by inflaming the optic nerve. While optic atrophy itself is not curable and damage to the optic nerve cannot be reversed, an early diagnosis may help prevent further vision loss if the underlying cause can be identified and corrected. Optic atrophy occurs most commonly in Denmark, affecting 1 in 10,000 people there.
Hemophilia jordan
Hemophilia is a genetic bleeding disorder caused by a defective gene on the X chromosome. People with hemophilia bleed excessively from minor cuts or bruises since their blood does not clot normally due to a missing clotting factor. While there is no cure, treatment involves replacing the missing clotting factor through injections to control bleeding. Hemophilia can be diagnosed through genetic testing and occurs in two main types, with Hemophilia A being more common.
Gb turner syndrome
Turner Syndrome is a genetic condition that affects development in females and is caused by the absence of one X chromosome. The effects at birth can include swollen hands, feet, and face. While there is no prevention or cure, doctors can test for it at birth through a karyotype and monitor development. Those with Turner Syndrome are typically shorter in height and may struggle with fertility, though pregnancy is possible with medical intervention.
Albinismbj
Albinism is a genetic condition caused by a lack of melanin pigment, resulting in white hair, pale skin, and vision problems. Both parents must carry the albinism gene for a child to inherit it. Those with albinism typically have white hair, blue or gray eyes with poor vision, milky white skin, and sensitivity to light. Treatments include wearing sunscreen, sunglasses, prescription lenses, eye surgery, and regular eye exams. While there is no prevention or cure, with proper care those with albinism can participate in normal activities and have vision, though risk of skin cancer is increased.
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Gb turner syndrome
- 2. Turner Syndrome ● This Henery H. Turner he was the founder of Turner Syndrome.
- 3. The Effects of Turner Syndrome ● The effects of turner syndrome is usually having swollen feet,hands,and face when born.
- 4. The Causes of Turner Syndrome ● The cause of Turner Syndrome is when the baby is born with one X chromosome. The other one is missing or has been damaged allong the way,like shown in the picture.
- 5. The Treatments of Turner Syndrome ● There are not any treatmernts to prevent Turner Syndrome but when the baby is born they can do at test called kayotype to see if the child will have Turner Syndrme.In some casses they can not tell until the child reaches puberty.
- 6. Intersting Facts ● ● ● Turner Syndrome effects 1 out of 2,000 people. Girls with Turner Syndrome the average height is 4 feet 7 inches. Girls with Turner Syndrome is is hard to get pregnant but can get pregnant by having a doctor plant a chromosome in the mother's womb.
- 7. Intersting Facts ● ● ● Turner Syndrome effects 1 out of 2,000 people. Girls with Turner Syndrome the average height is 4 feet 7 inches. Girls with Turner Syndrome is is hard to get pregnant but can get pregnant by having a doctor plant a chromosome in the mother's womb.