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Unit 3 Embryology
Clinically Oriented Anatomy (COA)
Texas Tech University Health Sciences Center
Created by Parker McCabe, Fall 2019
parker.mccabe@@uhsc.edu
Solu%ons
1. B
2. C
3. C
4. B
5. E
6. C
7. D
8. B
9. C
10. D
11. A
12. B
13. E
14. D
15. C
16. B
17. E
18. A
19. C
20. B
21. D
22. D
23. D
24. A
25. D
26. B
27. C
Digestive System
1. Which of the following structures develops as an outgrowth
of the endodermal epithelium of the upper part of the
duodenum?
A. Stomach
B. Pancreas
C. Lung buds
D. Trachea
E. Esophagus
Ques%on 1
A. Stomach- Foregut endoderm
B. Pancreas- The pancreas, liver, and biliary apparatus all develop from
outgrowths of the endodermal epithelium of the upper part of the
duodenum.
C. Lung buds- Foregut endoderm
D. Trachea- Foregut endoderm
E. Esophagus- Foregut endoderm
2. Where does the spleen originate and then end up after the
rotation of abdominal organs during fetal development?
A. Ventral mesentery à left side
B. Ventral mesentery à right side
C. Dorsal mesentery à left side
D. Dorsal mesentery à right side
E. It does not relocate
Question 2
A. Ventral mesentery à left side
B. Ventral mesentery à right side
C. Dorsal mesentery à left side- The spleen and dorsal pancreas are
embedded within the dorsal mesentery (greater omentum). After
rotation, dorsal will go to the left side of the body and ventral will
go to the right side of the body (except for the ventral pancreas).
D. Dorsal mesentery à right side
E. It does not relocate
3. After the first rotation of the stomach, which direction does
the right side now face and which nerve innervates it?
A. Posterior; left vagus nerve
B. Anterior; left vagus nerve
C. Posterior; right vagus nerve
D. Anterior; right vagus nerve
E. It doesn’t move until the second rotation of the stomach occurs
Ques%on 3
A. Posterior; le- vagus nerve
B. Anterior; le- vagus nerve
C. Posterior; right vagus nerve- The stomach rotates clockwise 90°
which puts the le- side facing anteriorly and the right side facing
posteriorly. Therefore, le- vagus nerve now innervates the anterior
wall and the right vagus nerve now innervates the posterior wall.
Remember LARP: Le- Anterior Right Posterior
D. Anterior; right vagus nerve
E. It doesn’t move unLl the second rotaLon of the stomach occurs
4. Which of the following organs is NOT secondary
retroperitoneal?
A. Pancreas
B. Kidneys
C. Duodenum
D. Ascending colon
E. Descending colon
Question 4
A. Pancreas
B. Kidneys- Secondary retroperitoneal means the organ once had a
mesentery and then lost it during development, while primary
retroperitoneal means the organ never had a mesentery. Remember
SAD PUCKER for the retroperitoneal organs: Suprarenal glands,
Aorta/IVC, Duodenum (2nd + 3rd parts), Pancreas (except for tail), Ureters,
Colon (ascending + descending), Kidneys, Esophagus, Rectum. Of these,
only the pancreas, duodenum, and colon are secondary. The rest are
primary.
C. Duodenum
D. Ascending colon
E. Descending colon
5. The umbilical vein is obliterated after birth to form the…
A. Coronary ligament
B. Median umbilical ligament
C. Right triangular ligament
D. Hepatoduodenal ligament
E. Round ligament of the liver
Ques%on 5
A. Coronary ligament
B. Median umbilical ligament- Embryological remnant of the urachus,
which is a remnant of the allantois.
C. Right triangular ligament
D. Hepatoduodenal ligament- The free margin of the lesser omentum
connecBng the liver and duodenum (hepatoduodenal ligament)
contains portal triad.
E. Round ligament of the liver- The free margin of the falciform
ligament contains the umbilical vein, which is obliterated aFer birth
to form the round ligament of the liver.
6. The primary intestinal loop remains in open connection with
the yolk sac via which structure?
A. Bile duct
B. Foramen of Winslow
C. Vitelline duct
D. Cystic duct
E. Portal triad
Question 6
A. Bile duct- Conveys bile to the duodenum; joins the cystic and
hepatic ducts.
B. Foramen of Winslow- Opening that connects the omental bursa
(lesser sac) to the rest of the peritoneal cavity (greater sac).
C. Vitelline duct
D. Cystic duct- Connects the neck of the gallbladder to the common
hepatic duct.
E. Portal triad- Hepatic portal vein, hepatic artery, and bile duct.
7. A neonate presents to the ED after projectile vomiting within an
hour of breastfeeding. The vomit is non-bilious and is a color that
resembles breast milk. What condition is likely present in the patient?
A. Esophageal atresia
B. Vitelline fistula
C. Duodenal atresia
D. Pyloric stenosis
E. Gastroschisis
Ques%on 7
A. Esophageal atresia- blind ended esophagus that prevents an infant from
swallowing food.
B. Vitelline fistula- Vitelline duct remains unobstructed over its en8re length, forming
a direct communica8on between the umbilicus and the intes8nal tract. A fecal
discharge may then be found in the umbilicus.
C. Duodenal atresia- Failure of the duodenum to recanalize and thus the lumen is
obstructed.
D. Pyloric stenosis- Muscle 8ssue in the pyloric sphincter hypertrophies resul8ng in
extreme narrowing of the pyloric lumen, obstruc8on of food passage and severe
projec8le vomi8ng.
E. Gastroschisis- Loops of bowel extend through a closure defect (most likely due to
abnormal closure of the body wall around the connec8ng stalk) in the ventral body
wall and are not covered by amnion.
8. Immediately after birth a newborn is found to have intestinal loops
outside of the body cavity that are still covered by amnion. The
patient has which of the following?
A. Gastroschisis
B. Omphalocele
C. Malrotation of the midgut loop
D. Hirschsprung’s Disease (megacolon)
E. Meckel’s or ileal diverticulum
Question 8
A. Gastroschisis- Loops of bowel extend through a closure defect (most
likely due to abnormal closure of the body wall around the connecting
stalk) in the ventral body wall and are not covered by amnion.
B. Omphalocele- Failure of the intestinal loops to return to the body cavity
after physiological herniation. The herniated loops are covered by the
amnion.
C. Malrotation of the midgut loop
D. Hirschsprung’s Disease (megacolon)
E. Meckel’s or ileal diverticulum- This is small pouch in the distal ileum
located on the anti-mesenteric side. It results when a remnant of the
vitelline duct persists from embryological development.
9. A patient presents to the ED complaining of sharp paraumbilical
pain radiating to the left lower quadrant and has a positive psoas sign
test. What is the likely diagnosis?
A. Gastroschisis
B. Annular pancreas
C. Appendicitis via malrotation of the midgut loop
D. Hirschsprung’s Disease (megacolon)
E. Meckel’s or ileal diverticulum
Ques%on 9
A. Gastroschisis
B. Annular pancreas
C. Appendici5s via malrota5on of the midgut loop- Malrota'on of the
midgut loop upon reentering the abdominal cavity can result in a
le8-sided colon, placing the ascending colon, cecum, and appendix
on the le8 side of the abdomen.
D. Hirschsprung’s Disease (megacolon)
E. Meckel’s or ileal diver5culum
10. During which week of embryonic development does the
cloacal membrane rupture?
A. 4th
B. 5th
C. 6th
D. 7th
E. 8th
Question 10
A. 4th
B. 5th
C. 6th
D. 7th -At the end of the 7th week, the cloacal membrane ruptures,
creating the anal opening for the hindgut and a ventral opening for
the urogenital sinus.
E. 8th
11. In the anal canal, the tissue superior to the pectinate line
is derived from which germ layer?
A. Endoderm
B. Ectoderm
C. Proctoderm-ectoderm
D. Neural crest cells
E. Mesoderm
Ques%on 11
A. Endoderm
B. Ectoderm
C. Proctoderm-ectoderm- The 3ssue inferior to the pec3nate line is
derived from proctoderm-ectoderm.
D. Neural crest cells
E. Mesoderm
12. A newborn is found to have a duodenum that is surrounded by
pancreatic tissue resulting in severe obstruction of the duodenum.
This newborn likely has…
A. Duodenal atresia
B. Annular Pancreas
C. Pancreatic divisum
D. Meckel’s diverticulum
E. Pyloric stenosis
Question 12
A. Duodenal atresia
B. Annular Pancreas- The right portion of the ventral pancreatic bud
migrates along its normal route while the left migrates in the opposite
direction. Thus, duodenum is surrounded by pancreatic tissue, resulting
in severe obstruction (choking) of the duodenum.
C. Pancreatic divisum- Pancreatic divisum is a congenital anomaly in the
anatomy of the ducts of the pancreas in which a single pancreatic duct is
not formed, but rather remains as two distinct dorsal and ventral ducts.
The majority of individuals born with pancreas divisum will not have
symptoms.
D. Meckel’s diverticulum
E. Pyloric stenosis
13. A newborn is found to have a congenital defect that is consistent
with the absence of parasympathetic innervation of the bowel wall.
This newborn likely has…
A. Meckel’s diverticulum
B. Omphalocele
C. Gastroschisis
D. Celiac’s disease
E. Hirschsprung’s Disease (megacolon)
Ques%on 13
A. Meckel’s diver/culum
B. Omphalocele
C. Gastroschisis
D. Celiac’s disease
E. Hirschsprung’s Disease (megacolon)- Due to a lack of
parasympathe2c innerva2on, the colon is unable to contract
properly producing a characteris2c swelling proximal to the neural
block.
Urinary System
14. The urinary system is derived from which germ layer?
A. Lateral plate Mesoderm
B. Endoderm
C. Ectoderm
D. Intermediate mesoderm
E. Neural crest cells
Question 14
A. Lateral plate Mesoderm
B. Endoderm
C. Ectoderm
D. Intermediate mesoderm
E. Neural crest cells
15. Which of the following renal structures originates from the
ureteric bud?
A. Proximal convoluted tubule
B. Bowman’s Capsule
C. Collec:ng ducts
D. Distal convoluted tubule
E. Loop of Henle
Ques%on 15
A. Proximal convoluted tubule- Forms from metanephric
mesoderm/blastema.
B. Bowman’s Capsule- Forms from metanephric mesoderm/blastema.
C. Collecting ducts- Forms from the ureteric bud which is an
outgrowth of the mesonephric duct.
D. Distal convoluted tubule- Forms from metanephric
mesoderm/blastema.
E. Loop of Henle- Forms from metanephric mesoderm /blastema.
16. The allantois goes on to immediately form which
structure?
A. Lateral umbilical ligament
B. Urachus
C. Median umbilical ligament
D. Medial umbilical ligament
E. Urethra
Question 16
A. Lateral umbilical ligament- Doesn’t exist. The inferior epigastric
artery lies beneath the lateral umbilical fold.
B. Urachus
C. Median umbilical ligament- Remnant of the urachus.
D. Medial umbilical ligament- Remnant of the umbilical artery.
E. Urethra
Reproductive System/Sexual
Differentiation
17. During which week of embryonic development do germ
cells first appear on the gonadal ridge?
A. 2nd
B. 3rd
C. 4th
D. 5th
E. 6th
Question 17
A. 2nd
B. 3rd
C. 4th
D. 5th
E. 6th- Germ cells do not appear in the gonadal ridges until the 6th
week of development.
18. Where do primordial germ cells (PGCs) originate?
A. Epiblast
B. Hypoblast
C. Primitive streak
D. Gonadal ridge
E. Yolk sac
Question 18
A. Epiblast- Primordial germ cells (PGCs) originate in the epiblast,
migrate through the primitive streak, and then reside in the yolk sac
close to the allantois. PGCs then migrate from the yolk sac into the
gonadal ridges.
B. Hypoblast
C. Primitive streak
D. Gonadal ridge
E. Yolk sac
19. The seminal vesicles are derived from which germ layer?
A. Ectoderm
B. Endoderm
C. Intermediate mesoderm
D. Lateral plate mesoderm
E. Neural crest cells
Question 19
A. Ectoderm
B. Endoderm
C. Intermediate mesoderm
D. Lateral plate mesoderm
E. Neural crest cells
20. A male newborn is found to have a non-functional 5a-reductase
enzyme. As a result, which of the following structures will fail to
develop properly until puberty?
A. Epididymis
B. Scrotum
C. Vas deferens
D. Efferent ductules
E. Seminal vesicles
Question 20
A. Epididymis
B. Scrotum- 5ά reductase is responsible for conver<ng testosterone into DHT,
which is a very “potent” form of testosterone that develops the external male
genitalia. When this enzyme is absent, it results in gene<c males looking like
liJle girls un<l puberty. Upon the onset of puberty, testosterone levels increase
(making up for the lack of DHT) and all of a sudden supposed “liJle girls” show
their true iden<ty as the external genitalia finally develop. In the Dominical
Republic this is known by the colloquial Spanish phrase, “huevos a los doce” or
“tes<cles at age twelve”. All other answer choices are s<mulated by
testosterone, which is unaffected by a lack of 5ά reductase or DHT.
C. Vas deferens
D. Efferent ductules
E. Seminal vesicles
21. A 23 year-old female presents to her primary care physician
sta7ng that she has been trying to get pregnant for over a year and
has been unsuccessful. Upon further exam, it is discovered that she
lacks oviducts and a uterus, and has abdominal testes. Which of the
following gene7c condi7ons is she likely suffering from?
A. Turner Syndrome
B. 5a-reductase deficiency
C. XX male
D. Androgen insensi;vity
E. Klinefelter Syndrome
Question 21
A. Turner Syndrome- This condition is characterized by a 45, XO genotype resulting in a female
that is generally underdeveloped.
B. 5a-reductase deficiency
C. XX male- This condition is due to a translocation of the SRY gene.
D. Androgen insensitivity- This condition results when a genetic XY male is unable to respond to
testosterone due to “insensitive” receptors. Testosterone is usually plentiful; however, it just
can’t do its job. As a result, the XY individual will look and act phenotypically female. Since the
testosterone produced from the testes is ineffective, the Mesonephric ducts (Wolffian) will
regress. However, anti- Mullerian hormone CAN still do its job, and the Mullerian ducts will
regress as well. This ultimately results in a genetic male that lives the lifestyle of a woman; she
just won’t be able to have children. (the loss of the Mullerian ducts leads to an absence of any
oviducts, a uterus, and the upper 1/3 of the vagina). It is also important to realize that the
androgen insensitivity causes the testes to remain in the abdomen where they develop
increasing the risk of testicular cancer.
E. Klinefelter Syndrome- This condition is characterized by a 47, XXY genotype resulting in a male
with small testes, low testosterone, and typically sterile.
22. A woman gives birth by cesarean section to two babies who were
thought to be twins. Upon further examination, it was found that the
woman had two separate uteruses, each occupied by its own baby,
with a common vaginal canal. Which of the following conditions does
the woman have?
A. Uterus didelphys
B. Uterus arcuatus
C. Klinefelter syndrome
D. Uterus bicornis
E. Turner syndrome
Question 22: page 251 in Langman’s Medical Embryology Textbook (12th ed.)-
Figure 16.31
A. Uterus didelphys- Uterus en)rely doubles.
B. Uterus arcuatus- Uterus is slightly indented in the middle.
C. Klinefelter syndrome- This condi)on is characterized by a 45, XO
genotype resul)ng in a female that is generally underdeveloped.
D. Uterus bicornis- Uterus has 2 horns entering a common vagina.
E. Turner syndrome- This condi)on is characterized by a 45, XO
genotype resul)ng in a female that is generally underdeveloped.
23. Which of the following structures arises from the
paramesonephric duct?
A. Labia
B. Prepuce of clitoris
C. Glans clitoris
D. Upper por9on of vagina
E. Lower por9on of vagina
Question 23
A. Labia
B. Prepuce of clitoris
C. Glans clitoris
D. Upper portion of vagina- The paramesonephric (Mullerian) ducts
give rise to the uterine tube, uterus, and upper portion of the
vagina. All other answer choices are external genitalia stimulated by
estrogen.
E. Lower portion of vagina
Lower Limb
24. Bones, joints, and fascia all originate from which embryonic
germ layer?
A. Lateral plate mesoderm
B. Intermediate mesoderm
C. Ectoderm
D. Endoderm
E. Neural crest cells
Ques%on 24
A. Lateral plate mesoderm- Bones, joints, and fascia come from lateral
plate mesoderm.
B. Intermediate mesoderm
C. Ectoderm
D. Endoderm
E. Neural crest cells
25. Dermatomes in the lower limb twist ______ as opposed to
______ in the upper limb.
A. Anteriorly; posteriorly
B. Posteriorly; anteriorly
C. Laterally; medially
D. Medially; laterally
E. Dermatomes only twist in the lower limbs.
Question 25
A. Anteriorly; posteriorly
B. Posteriorly; anteriorly
C. Laterally; medially
D. Medially; laterally- Dermatomes twist medially in the lower limb as
opposed to laterally in the upper limb.
E. Dermatomes only twist in the lower limbs.
Amniotic Fluid, Circulation, and
Placental Membranes
26. Which of the following is not a layer of the chorionic villi?
A. Chorionic blood vessels
B. Placenta
C. Cytotrophoblast
D. Syncy9otrophoblast
E. Extra-embryonic mesoderm
Ques%on 26
A. Chorionic blood vessels
B. Placenta- The chorionic villi are made up of three layers. From
inside to outside: the chorionic blood vessels (extra-embryonic
mesoderm), the cytotrophoblast, and the syncyBotrophoblast.
C. Cytotrophoblast
D. SyncyBotrophoblast
E. Extra-embryonic mesoderm
27. The ______ becomes the maternal portion of the
placenta.
A. Blastocyst
B. Trophoblast
C. Decidua basalis
D. Decidua capsularis
E. Decidua parietalis
Question 27
A. Blastocyst
B. Trophoblast
C. Decidua basalis- The decidua is a nutrient/vascular rich region of
the endometrium inside the uterus where the blastocyst implants.
The decidua basalis becomes the maternal portion of the placenta.
D. Decidua capsularis- The decidua capsularis is the decidual lining
overriding the implanted blastocyst.
E. Decidua parietalis- The decidua parietalis is the layer that doesn’t
surround the implanted blastocyst directly.

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COA Unit 3 Embryology

  • 1. Unit 3 Embryology Clinically Oriented Anatomy (COA) Texas Tech University Health Sciences Center Created by Parker McCabe, Fall 2019 parker.mccabe@@uhsc.edu
  • 2. Solu%ons 1. B 2. C 3. C 4. B 5. E 6. C 7. D 8. B 9. C 10. D 11. A 12. B 13. E 14. D 15. C 16. B 17. E 18. A 19. C 20. B 21. D 22. D 23. D 24. A 25. D 26. B 27. C
  • 4. 1. Which of the following structures develops as an outgrowth of the endodermal epithelium of the upper part of the duodenum? A. Stomach B. Pancreas C. Lung buds D. Trachea E. Esophagus
  • 5. Ques%on 1 A. Stomach- Foregut endoderm B. Pancreas- The pancreas, liver, and biliary apparatus all develop from outgrowths of the endodermal epithelium of the upper part of the duodenum. C. Lung buds- Foregut endoderm D. Trachea- Foregut endoderm E. Esophagus- Foregut endoderm
  • 6. 2. Where does the spleen originate and then end up after the rotation of abdominal organs during fetal development? A. Ventral mesentery à left side B. Ventral mesentery à right side C. Dorsal mesentery à left side D. Dorsal mesentery à right side E. It does not relocate
  • 7. Question 2 A. Ventral mesentery à left side B. Ventral mesentery à right side C. Dorsal mesentery à left side- The spleen and dorsal pancreas are embedded within the dorsal mesentery (greater omentum). After rotation, dorsal will go to the left side of the body and ventral will go to the right side of the body (except for the ventral pancreas). D. Dorsal mesentery à right side E. It does not relocate
  • 8. 3. After the first rotation of the stomach, which direction does the right side now face and which nerve innervates it? A. Posterior; left vagus nerve B. Anterior; left vagus nerve C. Posterior; right vagus nerve D. Anterior; right vagus nerve E. It doesn’t move until the second rotation of the stomach occurs
  • 9. Ques%on 3 A. Posterior; le- vagus nerve B. Anterior; le- vagus nerve C. Posterior; right vagus nerve- The stomach rotates clockwise 90° which puts the le- side facing anteriorly and the right side facing posteriorly. Therefore, le- vagus nerve now innervates the anterior wall and the right vagus nerve now innervates the posterior wall. Remember LARP: Le- Anterior Right Posterior D. Anterior; right vagus nerve E. It doesn’t move unLl the second rotaLon of the stomach occurs
  • 10. 4. Which of the following organs is NOT secondary retroperitoneal? A. Pancreas B. Kidneys C. Duodenum D. Ascending colon E. Descending colon
  • 11. Question 4 A. Pancreas B. Kidneys- Secondary retroperitoneal means the organ once had a mesentery and then lost it during development, while primary retroperitoneal means the organ never had a mesentery. Remember SAD PUCKER for the retroperitoneal organs: Suprarenal glands, Aorta/IVC, Duodenum (2nd + 3rd parts), Pancreas (except for tail), Ureters, Colon (ascending + descending), Kidneys, Esophagus, Rectum. Of these, only the pancreas, duodenum, and colon are secondary. The rest are primary. C. Duodenum D. Ascending colon E. Descending colon
  • 12. 5. The umbilical vein is obliterated after birth to form the… A. Coronary ligament B. Median umbilical ligament C. Right triangular ligament D. Hepatoduodenal ligament E. Round ligament of the liver
  • 13. Ques%on 5 A. Coronary ligament B. Median umbilical ligament- Embryological remnant of the urachus, which is a remnant of the allantois. C. Right triangular ligament D. Hepatoduodenal ligament- The free margin of the lesser omentum connecBng the liver and duodenum (hepatoduodenal ligament) contains portal triad. E. Round ligament of the liver- The free margin of the falciform ligament contains the umbilical vein, which is obliterated aFer birth to form the round ligament of the liver.
  • 14. 6. The primary intestinal loop remains in open connection with the yolk sac via which structure? A. Bile duct B. Foramen of Winslow C. Vitelline duct D. Cystic duct E. Portal triad
  • 15. Question 6 A. Bile duct- Conveys bile to the duodenum; joins the cystic and hepatic ducts. B. Foramen of Winslow- Opening that connects the omental bursa (lesser sac) to the rest of the peritoneal cavity (greater sac). C. Vitelline duct D. Cystic duct- Connects the neck of the gallbladder to the common hepatic duct. E. Portal triad- Hepatic portal vein, hepatic artery, and bile duct.
  • 16. 7. A neonate presents to the ED after projectile vomiting within an hour of breastfeeding. The vomit is non-bilious and is a color that resembles breast milk. What condition is likely present in the patient? A. Esophageal atresia B. Vitelline fistula C. Duodenal atresia D. Pyloric stenosis E. Gastroschisis
  • 17. Ques%on 7 A. Esophageal atresia- blind ended esophagus that prevents an infant from swallowing food. B. Vitelline fistula- Vitelline duct remains unobstructed over its en8re length, forming a direct communica8on between the umbilicus and the intes8nal tract. A fecal discharge may then be found in the umbilicus. C. Duodenal atresia- Failure of the duodenum to recanalize and thus the lumen is obstructed. D. Pyloric stenosis- Muscle 8ssue in the pyloric sphincter hypertrophies resul8ng in extreme narrowing of the pyloric lumen, obstruc8on of food passage and severe projec8le vomi8ng. E. Gastroschisis- Loops of bowel extend through a closure defect (most likely due to abnormal closure of the body wall around the connec8ng stalk) in the ventral body wall and are not covered by amnion.
  • 18. 8. Immediately after birth a newborn is found to have intestinal loops outside of the body cavity that are still covered by amnion. The patient has which of the following? A. Gastroschisis B. Omphalocele C. Malrotation of the midgut loop D. Hirschsprung’s Disease (megacolon) E. Meckel’s or ileal diverticulum
  • 19. Question 8 A. Gastroschisis- Loops of bowel extend through a closure defect (most likely due to abnormal closure of the body wall around the connecting stalk) in the ventral body wall and are not covered by amnion. B. Omphalocele- Failure of the intestinal loops to return to the body cavity after physiological herniation. The herniated loops are covered by the amnion. C. Malrotation of the midgut loop D. Hirschsprung’s Disease (megacolon) E. Meckel’s or ileal diverticulum- This is small pouch in the distal ileum located on the anti-mesenteric side. It results when a remnant of the vitelline duct persists from embryological development.
  • 20. 9. A patient presents to the ED complaining of sharp paraumbilical pain radiating to the left lower quadrant and has a positive psoas sign test. What is the likely diagnosis? A. Gastroschisis B. Annular pancreas C. Appendicitis via malrotation of the midgut loop D. Hirschsprung’s Disease (megacolon) E. Meckel’s or ileal diverticulum
  • 21. Ques%on 9 A. Gastroschisis B. Annular pancreas C. Appendici5s via malrota5on of the midgut loop- Malrota'on of the midgut loop upon reentering the abdominal cavity can result in a le8-sided colon, placing the ascending colon, cecum, and appendix on the le8 side of the abdomen. D. Hirschsprung’s Disease (megacolon) E. Meckel’s or ileal diver5culum
  • 22. 10. During which week of embryonic development does the cloacal membrane rupture? A. 4th B. 5th C. 6th D. 7th E. 8th
  • 23. Question 10 A. 4th B. 5th C. 6th D. 7th -At the end of the 7th week, the cloacal membrane ruptures, creating the anal opening for the hindgut and a ventral opening for the urogenital sinus. E. 8th
  • 24. 11. In the anal canal, the tissue superior to the pectinate line is derived from which germ layer? A. Endoderm B. Ectoderm C. Proctoderm-ectoderm D. Neural crest cells E. Mesoderm
  • 25. Ques%on 11 A. Endoderm B. Ectoderm C. Proctoderm-ectoderm- The 3ssue inferior to the pec3nate line is derived from proctoderm-ectoderm. D. Neural crest cells E. Mesoderm
  • 26. 12. A newborn is found to have a duodenum that is surrounded by pancreatic tissue resulting in severe obstruction of the duodenum. This newborn likely has… A. Duodenal atresia B. Annular Pancreas C. Pancreatic divisum D. Meckel’s diverticulum E. Pyloric stenosis
  • 27. Question 12 A. Duodenal atresia B. Annular Pancreas- The right portion of the ventral pancreatic bud migrates along its normal route while the left migrates in the opposite direction. Thus, duodenum is surrounded by pancreatic tissue, resulting in severe obstruction (choking) of the duodenum. C. Pancreatic divisum- Pancreatic divisum is a congenital anomaly in the anatomy of the ducts of the pancreas in which a single pancreatic duct is not formed, but rather remains as two distinct dorsal and ventral ducts. The majority of individuals born with pancreas divisum will not have symptoms. D. Meckel’s diverticulum E. Pyloric stenosis
  • 28. 13. A newborn is found to have a congenital defect that is consistent with the absence of parasympathetic innervation of the bowel wall. This newborn likely has… A. Meckel’s diverticulum B. Omphalocele C. Gastroschisis D. Celiac’s disease E. Hirschsprung’s Disease (megacolon)
  • 29. Ques%on 13 A. Meckel’s diver/culum B. Omphalocele C. Gastroschisis D. Celiac’s disease E. Hirschsprung’s Disease (megacolon)- Due to a lack of parasympathe2c innerva2on, the colon is unable to contract properly producing a characteris2c swelling proximal to the neural block.
  • 31. 14. The urinary system is derived from which germ layer? A. Lateral plate Mesoderm B. Endoderm C. Ectoderm D. Intermediate mesoderm E. Neural crest cells
  • 32. Question 14 A. Lateral plate Mesoderm B. Endoderm C. Ectoderm D. Intermediate mesoderm E. Neural crest cells
  • 33. 15. Which of the following renal structures originates from the ureteric bud? A. Proximal convoluted tubule B. Bowman’s Capsule C. Collec:ng ducts D. Distal convoluted tubule E. Loop of Henle
  • 34. Ques%on 15 A. Proximal convoluted tubule- Forms from metanephric mesoderm/blastema. B. Bowman’s Capsule- Forms from metanephric mesoderm/blastema. C. Collecting ducts- Forms from the ureteric bud which is an outgrowth of the mesonephric duct. D. Distal convoluted tubule- Forms from metanephric mesoderm/blastema. E. Loop of Henle- Forms from metanephric mesoderm /blastema.
  • 35. 16. The allantois goes on to immediately form which structure? A. Lateral umbilical ligament B. Urachus C. Median umbilical ligament D. Medial umbilical ligament E. Urethra
  • 36. Question 16 A. Lateral umbilical ligament- Doesn’t exist. The inferior epigastric artery lies beneath the lateral umbilical fold. B. Urachus C. Median umbilical ligament- Remnant of the urachus. D. Medial umbilical ligament- Remnant of the umbilical artery. E. Urethra
  • 38. 17. During which week of embryonic development do germ cells first appear on the gonadal ridge? A. 2nd B. 3rd C. 4th D. 5th E. 6th
  • 39. Question 17 A. 2nd B. 3rd C. 4th D. 5th E. 6th- Germ cells do not appear in the gonadal ridges until the 6th week of development.
  • 40. 18. Where do primordial germ cells (PGCs) originate? A. Epiblast B. Hypoblast C. Primitive streak D. Gonadal ridge E. Yolk sac
  • 41. Question 18 A. Epiblast- Primordial germ cells (PGCs) originate in the epiblast, migrate through the primitive streak, and then reside in the yolk sac close to the allantois. PGCs then migrate from the yolk sac into the gonadal ridges. B. Hypoblast C. Primitive streak D. Gonadal ridge E. Yolk sac
  • 42. 19. The seminal vesicles are derived from which germ layer? A. Ectoderm B. Endoderm C. Intermediate mesoderm D. Lateral plate mesoderm E. Neural crest cells
  • 43. Question 19 A. Ectoderm B. Endoderm C. Intermediate mesoderm D. Lateral plate mesoderm E. Neural crest cells
  • 44. 20. A male newborn is found to have a non-functional 5a-reductase enzyme. As a result, which of the following structures will fail to develop properly until puberty? A. Epididymis B. Scrotum C. Vas deferens D. Efferent ductules E. Seminal vesicles
  • 45. Question 20 A. Epididymis B. Scrotum- 5ά reductase is responsible for conver<ng testosterone into DHT, which is a very “potent” form of testosterone that develops the external male genitalia. When this enzyme is absent, it results in gene<c males looking like liJle girls un<l puberty. Upon the onset of puberty, testosterone levels increase (making up for the lack of DHT) and all of a sudden supposed “liJle girls” show their true iden<ty as the external genitalia finally develop. In the Dominical Republic this is known by the colloquial Spanish phrase, “huevos a los doce” or “tes<cles at age twelve”. All other answer choices are s<mulated by testosterone, which is unaffected by a lack of 5ά reductase or DHT. C. Vas deferens D. Efferent ductules E. Seminal vesicles
  • 46. 21. A 23 year-old female presents to her primary care physician sta7ng that she has been trying to get pregnant for over a year and has been unsuccessful. Upon further exam, it is discovered that she lacks oviducts and a uterus, and has abdominal testes. Which of the following gene7c condi7ons is she likely suffering from? A. Turner Syndrome B. 5a-reductase deficiency C. XX male D. Androgen insensi;vity E. Klinefelter Syndrome
  • 47. Question 21 A. Turner Syndrome- This condition is characterized by a 45, XO genotype resulting in a female that is generally underdeveloped. B. 5a-reductase deficiency C. XX male- This condition is due to a translocation of the SRY gene. D. Androgen insensitivity- This condition results when a genetic XY male is unable to respond to testosterone due to “insensitive” receptors. Testosterone is usually plentiful; however, it just can’t do its job. As a result, the XY individual will look and act phenotypically female. Since the testosterone produced from the testes is ineffective, the Mesonephric ducts (Wolffian) will regress. However, anti- Mullerian hormone CAN still do its job, and the Mullerian ducts will regress as well. This ultimately results in a genetic male that lives the lifestyle of a woman; she just won’t be able to have children. (the loss of the Mullerian ducts leads to an absence of any oviducts, a uterus, and the upper 1/3 of the vagina). It is also important to realize that the androgen insensitivity causes the testes to remain in the abdomen where they develop increasing the risk of testicular cancer. E. Klinefelter Syndrome- This condition is characterized by a 47, XXY genotype resulting in a male with small testes, low testosterone, and typically sterile.
  • 48. 22. A woman gives birth by cesarean section to two babies who were thought to be twins. Upon further examination, it was found that the woman had two separate uteruses, each occupied by its own baby, with a common vaginal canal. Which of the following conditions does the woman have? A. Uterus didelphys B. Uterus arcuatus C. Klinefelter syndrome D. Uterus bicornis E. Turner syndrome
  • 49. Question 22: page 251 in Langman’s Medical Embryology Textbook (12th ed.)- Figure 16.31 A. Uterus didelphys- Uterus en)rely doubles. B. Uterus arcuatus- Uterus is slightly indented in the middle. C. Klinefelter syndrome- This condi)on is characterized by a 45, XO genotype resul)ng in a female that is generally underdeveloped. D. Uterus bicornis- Uterus has 2 horns entering a common vagina. E. Turner syndrome- This condi)on is characterized by a 45, XO genotype resul)ng in a female that is generally underdeveloped.
  • 50. 23. Which of the following structures arises from the paramesonephric duct? A. Labia B. Prepuce of clitoris C. Glans clitoris D. Upper por9on of vagina E. Lower por9on of vagina
  • 51. Question 23 A. Labia B. Prepuce of clitoris C. Glans clitoris D. Upper portion of vagina- The paramesonephric (Mullerian) ducts give rise to the uterine tube, uterus, and upper portion of the vagina. All other answer choices are external genitalia stimulated by estrogen. E. Lower portion of vagina
  • 53. 24. Bones, joints, and fascia all originate from which embryonic germ layer? A. Lateral plate mesoderm B. Intermediate mesoderm C. Ectoderm D. Endoderm E. Neural crest cells
  • 54. Ques%on 24 A. Lateral plate mesoderm- Bones, joints, and fascia come from lateral plate mesoderm. B. Intermediate mesoderm C. Ectoderm D. Endoderm E. Neural crest cells
  • 55. 25. Dermatomes in the lower limb twist ______ as opposed to ______ in the upper limb. A. Anteriorly; posteriorly B. Posteriorly; anteriorly C. Laterally; medially D. Medially; laterally E. Dermatomes only twist in the lower limbs.
  • 56. Question 25 A. Anteriorly; posteriorly B. Posteriorly; anteriorly C. Laterally; medially D. Medially; laterally- Dermatomes twist medially in the lower limb as opposed to laterally in the upper limb. E. Dermatomes only twist in the lower limbs.
  • 57. Amniotic Fluid, Circulation, and Placental Membranes
  • 58. 26. Which of the following is not a layer of the chorionic villi? A. Chorionic blood vessels B. Placenta C. Cytotrophoblast D. Syncy9otrophoblast E. Extra-embryonic mesoderm
  • 59. Ques%on 26 A. Chorionic blood vessels B. Placenta- The chorionic villi are made up of three layers. From inside to outside: the chorionic blood vessels (extra-embryonic mesoderm), the cytotrophoblast, and the syncyBotrophoblast. C. Cytotrophoblast D. SyncyBotrophoblast E. Extra-embryonic mesoderm
  • 60. 27. The ______ becomes the maternal portion of the placenta. A. Blastocyst B. Trophoblast C. Decidua basalis D. Decidua capsularis E. Decidua parietalis
  • 61. Question 27 A. Blastocyst B. Trophoblast C. Decidua basalis- The decidua is a nutrient/vascular rich region of the endometrium inside the uterus where the blastocyst implants. The decidua basalis becomes the maternal portion of the placenta. D. Decidua capsularis- The decidua capsularis is the decidual lining overriding the implanted blastocyst. E. Decidua parietalis- The decidua parietalis is the layer that doesn’t surround the implanted blastocyst directly.