Young's Embryology MCQs Flashcards

1
Q
  1. Anorectal agenesis is more common in males than females and is usually associated with a rectourethral fistula. The embryological basis of the fistula is
A. abnormal partitioning of the cloaca
B. agenesis of the urorectal septum
C. failure of fixation of the hindgut
D. failure of the proctodeum  to develop
E. premature rupture of the anal membrane
A

A

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2
Q
  1. The junction of the endodermal epithelium of the hindgut and the ectoderm of the proctodeum or anal pit is believed to be indicated by the
A. external sphincter 
B. levator ani muscles 
C. pectinate line
D. superior ends of the anal columns
E white line
A

C

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3
Q
  1. Massive rectal bleeding was observed in an infant. The color of the blood ranged from bright to dark red. The child appeared to be free of any pain. A diagnosis of Meckel’s diverticulum was made. This condition is associated with which of the following?
A. Duplication of the intestine. 
B. Herniation of the intestines. 
C. Remnant of the yolk stalk. 
D. Nonrotation of the midgut.
E. Subhepatic cecum and appendix.
A

C

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4
Q
  1. As the stomach acquires its adult shape, it rotates around its longitudinal axis. Which of the following events does not result from this rotation?

A. The ventral border of the stomach moves to the right.
B. The dorsal border of the stomach moves to the left.
C. The dorsal mesogastrium is carried to the left.
D. The duodenum rotates to the right.
E. The dorsal part of the stomach grows rapidly.

A

E

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5
Q
  1. Which of the following is the most common type of anorectal malformation?
A. Anal agenesis
B. Anorectal agenesis
C. Anal stenosis
D. Ectopic anus
E. Persistant anal membrane
A

B

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6
Q
  1. The anal membrane usually ruptures at the end of the week.
A. 5th 
B. 6th 
C. 7th 
D. 8th
E. 9th
A

C

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7
Q
  1. Pyloric stenosis is characterized by vomiting, usually starting in the second or third week after birth, which becomes increasingly projectile. The narrowing of the pyloric lumen results primarily from:

A. a diaphragm-like narrowing of the pyloric lumen
B. a so-called “fetal vascular accident” in the pylorus
C. hypertrophy of the circular muscle layer
D. hypertrophy of the longitudinal muscle layer
E. persistence of the solid stage of pyloric development

A

C

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8
Q
  1. When the primary intestinal loop undergoes rotation between weeks 6 and 11, which of the following blood vessels lies along the axis around which it rotates ?
A. abdominal aorta
B. celiac artery
C. inferior mesenteric artery
D. left umbilical vein
E. superior mesenteric artery
A

E

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9
Q
  1. In a baby born with reversed rotation of the midgut, the duodenum lies ventral to the transverse colon. In the embryogenesis of this malformation, the primary intestinal loop (viewed from in front) accomplishes a net rotation around its long axis of how many degrees and in which direction?
A. 90 degrees clockwise
B. 90 degrees counterclockwise
C. 180 degrees clockwise
D. 270 degrees counterclockwise
E. 270 degrees clockwise
A

A

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10
Q
  1. An infant is born with a mid-ventral defect of the abdominal wall of the type that is often attributed to a failure of the umbilical ring to close. The viscera that protrude through this defect are covered with amniotic membrane alone. A term for this infant’s malformation is
A. cloacal exstrophy
B. epispadias
C. gastroschisis 
D. meningocele 
E. omphalocele
A

E

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11
Q
  1. An infant is born with an abdominal wall defect that is located just to the right of the umbilicus. The protruding viscera is covered by neither amniotic membrane nor parietal peritoneum. A term for this infant’s malformation is
A. epispadias
B. gastroschisis
C. omphalocele
D. omphalomesenteric fistula
E. urachal fistula
A

B

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12
Q
  1. Delay in passage of meconium was noted in a male infant. Additional symptoms included constipation, vomiting, and abdominal distention. A barium enema and x-rays revealed a distended sigmoid colon and a nonperistaltic rectum. Pathology reported a normal number of parasympathetic ganglion cells in the sigmoid colon. A diagnosis of congenital megacolon (Hirschsprung’s disease) was made. This condition is associated with which of the following?

A. failure of the endodermal cells to line the colonic cavity
B. failure of neural crest cells to migrate forming the enteric parasympathetic ganglia
C. failure to recanalize the intestine
D. hypertrophy of myoblasts forming the inner circular layer of smooth muscle
E. hypertrophy of myoblasts forming the outer longitudinal layer of smooth muscle

A

B

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13
Q
  1. An infant is born with a defect in the umbilicus that exposes intestinal mucosa and oozes meconium. A term for this infant’s malformation is
A. gastroschisis 
B. meningocele 
C. omphalocele
D. omphalomesenteric fistula
E. urachal fistula
A

D

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14
Q
  1. The teeth of an 8-year-old child were badly discolored, giving them a brownish yellow appearance, and the enamel was hypoplastic. This condition is usually associated with which of the following?
A. congenital syphilis
E. diazepam
D. herpes simplex virus
C. phenytoin
B. tetracyclines
A

B

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15
Q
  1. In humans, cleft lip, with or without cleft palate, usually results from
A. cortisone
B. infectious disease
C. radiation
D. rubella virus
E. trimethadione
A

E

Trimethadione is an oxazolidinedione anticonvulsant. It is most commonly used to treat epileptic conditions that are resistant to other treatments.

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16
Q
  1. Narrowing of the lumen in pyloric stenosis usually results from

A. a diaphragm-like narrowing of the pyloric lumen B. a so-called “fetal vascular accident” in the pylorus
C. hypertrophy of the circular muscle layer
D. hypertrophy of the longitudinal muscle layer
E. persistence of the solid stage of pyloric development

A

C

17
Q
  1. Which of the following is the most common congenital anomaly of the head and neck?
A. bilateral cleft lip
B. cleft palate
C. median cleft lip
D. oblique facial cleft
E. unilateral cleft lip
A

E

18
Q
  1. A young infant had a small blind pit on the side of the neck along the anterior border of the sternocleidomastoid muscle. Mucus dripped intermittantly from its opening. What is the most likely embryologic basis of this congenital anomaly of the neck? Persistence of the embryonic opening of the
A. second groove and cervical sinus
B. second pharyngeal pouch
C. second pouch and groove
D. third branchial groove
E. thyroglossal duct
A

A

19
Q
  1. The major portion of the human palate develops from the
A. frontonasal elevation
B. intermaxillary segment 
C. lateral palatine process 
D. medial nasal prominences 
E. median palatine process
A

C

20
Q
  1. In DiGeorge syndrome, the development of the thymus is affected. Which of the following pharyngeal pouch is involved?
A. 1st 
B. 2nd 
C. 3rd 
D. 4th 
E. 5th
A

C

21
Q
  1. When the palatine processes (palatal shelves) fail to meet and fuse with each other and with the nasal septum, the resulting anomaly is a cleft of which of the following?
A. intermaxillary segment
B. primary and secondary palates
C. primary palate
D. secondary palate
E. uvula
A

D

22
Q
  1. The greater cornu and the inferior part of the hyoid bone were absent at birth. Which of the following embryonic structures was affected?
A. fourth branchial (pharyngeal) arch
B. mandibular prominence
C. maxillary prominence
D. second branchial (pharyngeal) arch
E. third branchial (pharyngeal) arch
A

E

23
Q
  1. The intraembryonic coelom (embryonic body cavity) is first recognizable during the which week after fertilization?
A. 2nd 
B. 3rd 
C. 4th 
D. 5th 
E. 6th
A

B

24
Q
  1. The first component of the developing diaphragm is recognizable at the end of the which week of development?
A. 2nd 
B. 3rd 
C. 4th 
D. 5th 
E. 6th
A

B

25
Q
  1. After folding of the embryo, the dorsal mesentary extends from the

A. caudal part of the esophagus to the cloacal region
B. caudal part of the foregut to the cranial part of the hindgut
C. cranial part of the esophagus to the cloacal region
D. cranial part of the foregut to the caudal region
E. stomodeum to the proctodeum

A

A

26
Q
  1. In a 4-week embryo, the developing diaphragm (represented by the septum transversum) is located at the level of which somites?
A. inferior thoracic
B. intermediate cervical
C. superior thoracic
D. lumbar
E. sacral
A

B

27
Q
  1. Most of the muscle forming cells (myoblasts) that give rise to the musculature of the diaphragm are derived from mesodermal cells that originate in which structure?
A. central tendon
B. peripheral portions
C. posterolateral portions
D. right and left cura
E. septum transversum
A

D

28
Q
  1. The septum transversum gives rise to which portion of the diaphragm?
A. central tendon
B. peripheral portions
C. posterolateral portions
D. right and left cura
E. small intermediate portions
A

D

29
Q
  1. The pleuroperitoneal membranes gives rise to which portion of the diaphragm?
A. central tendon
B. peripheral portions
C. posterolateral portions
D. right and left cura
E. small intermediate portions
A

E

30
Q
  1. The growth of muscle fibers into the dorsal mesentery of the esophagus gives rise to which portion of the diaphragm.
A. central tendon
B. peripheral portions
C. posterolateral portions
D. right and left cura
E. small intermediate portions
A

D

31
Q
  1. In a 5-week embryo, the ventral mesentery of the primitive gut disappears, except where it is attached to what structure?
A. caudal region of the foregut 
B. caudal region of the hindgut 
C. cranial region of the midgut
D. embryonic part of the yolk sac
E. primitive pharynx
A

A

32
Q
  1. A congenital diaphragmatic hernia (CDH) was diagnosed prenatally by ultrasonography. Which of the following structures was probably involved?
A. costodiaphragmatic recess
B. dorsal mesentry of the esophagus
C. lateral body wall
D. pleuroperitoneal membrane
E. septum transversum
A

D

33
Q
  1. Delay in passage of meconium was noted in a male infant. Additional symptoms included constipation, vomiting, and abdominal distention. A barium enema and x-rays revealed a distended sigmoid colon and a nonperistaltic rectum. Pathology reported a normal number of parasympathetic ganglion cells in the sigmoid colon. A diagnosis of congenital megacolon (Hirschsprung’s disease) was made. This condition is associated with which of the following?
A. failure of neural crest cells to migrate into wall of rectum
B. failure to recanalize the intestine
C. gastroschisis
D. imperforate anus
E. midgut volvulus
A

A

34
Q
  1. A sonogram of a 20-week-old male fetus demonstrated abdominal viscera within the amniotic cavity. Subsequent high-resolution sonogram at 22 weeks showed a defect in the abdominal wall of the fetus to the right of the umbilical cord with extrusion of intestinal loops into the amniotic cavity. Identify the MOST LIKELY diagnosis for this fetus.
A. congenital omphalocoele
B. gastroschisis
C. mobile cecum
D. subhepatic cecum and appendix
E. umbilical hernia
A

B

35
Q
  1. A newborn presented with respiratory distress. The newborn appeared normal at birth, but after a few swallows regurgitated fluid through nose and mouth. There was inability to pass a nasogastric tube through the esophagus into the stomach. Radiographic examination demonstrated the nasogastric tube in a proximal esophageal pouch. A diagnosis of esophageal atresia was made. The germ layer most affected in this instance is the
A. endoderm
B. intermediate mesoderm
C. neural crest
D. neural ectoderm
E. surface ectoderm
A

A

36
Q
  1. A 60-year-old male presents with signs and symptoms of an acute appendicitis. History, physical exam, and labs reveal inflammation of the area around the umbilicus, with ulceration and internal bleeding along the antimesenteric border of the ileum. A provisional diagnosis of
    Ileal (Meckel) Diverticulum was made. Identify the embryological remnant that this diverticulum represents.
A. distal portion of the allantois
B. distal portion of the yolk stalk
C. proximal portion of the allantois
D. proximal portion of the midgut
E. proximal portion of the yolk stalk
A

E

37
Q
  1. An infant presents with projectile vomiting. A barium swallow indicates a distended stomach with severe stenosis of the pyloric canal and obstruction to the passage of food into the duodenum. This condition is due to abnormal development of which embryonic layer?
A. endoderm
B. lateral plate somatic mesoderm
C. lateral plate splanchnic mesoderm
D. neural crest
E. neural ectoderm
A

C

38
Q
  1. A baby is born with a nonrotation of the intestines, meaning in this case that the primary intestinal loop underwent only a single, initial rotation of 90 degrees counterclockwise when viewed in the front. Which of the following statements best describes the disposition of the baby’s small and large intestines relative to each other in the abdominal cavity?

A. The small and large intestines are both distributed equally in the left and right sides of the abdominal cavity.
B. The small and large intestines are together in the left side of the abdominal cavity.
C. The small and large intestines are together in the right side of the abdominal cavity.
D. The small intestine is in the left side and the large intestine is in the right side of the abdominal cavity.
E. The small intestine is in the right side and the large intestine is in the left side of the abdominal cavity.

A

E