Embryology II Flashcards

1
Q

When are the neuropores expected to fuse together?

A

At the fourth week of gestation (p.409)

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2
Q

What occurs if the neuropores do not fuse together at the fourth week of gestation?

A

Neural tube defects (p.409)

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3
Q

What is a neural tube defect?

A

A persistent connection between the amniotic cavity and spinal canal (p.409)

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4
Q

What amniotic fluid and maternal serum protein is elevated in the instance of a neural tube defect?

A

Elevated a-fetoprotein (AFP) (p.409)

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5
Q

What amniotic protein is used to confirm a neural tube defect in a fetus?

A

Elevated acetylcholinesterase (p.409)

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6
Q

What is spina bifida occulta?

A

Failure of the spinal canal to close without structural herniation; dura is intact (p.409)

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7
Q

Where is spina bifida occulta usually seen?

A

At the lower vertebral levels (p.409)

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8
Q

What physical findings are associated with spina bifida occulta?

A

A tuft of hair or skin dimple at the level of the bony defect (p.409)

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9
Q

What is a meningocele?

A

When the meninges (but not the spinal cord) herniate through the spinal canal defect (p.409)

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10
Q

What is a meningomyelocele?

A

When the meninges and spinal cord herniate through the spinal canal defect (p.409)

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11
Q

Name three neural tube defects.

A

Spina bifida occulta, meningocele, meningomyelocele (p.409)

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12
Q

Name two forebrain embryologic anomalies.

A

Anencephaly, holoprosencephaly (p.409)

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13
Q

What is anencephaly?

A

Malformation of the anterior neural tube resulting in no forevrain and open calvarium (p.409)

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14
Q

What are the clinical findings associated with anencephaly?

A

Increased a-fetoprotein, polyhydraminos (no swallowing centre in the brain) (p.409)

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15
Q

What maternal condition is associated with anencephaly?

A

DM type I (p.409)

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16
Q

What can decrease maternal risk of a fetus with anencephaly?

A

Folate supplementation (p.409)

17
Q

What is holoprosencephaly?

A

Failure of left and right hemispheres to separate (p.409)

18
Q

When does holoprosencephaly occur in a fetus?

A

During weeks 5-6 (p.409)

19
Q

What is the etiology of holoprosencephaly?

A

Multifactorial; may be related to mutations in sonic hedgehog signaling pathway (p.409)

20
Q

Name a common clinical finding associated with mild holoprosencephaly.

A

Cleft lip/palate (p.409)

21
Q

Name a common clinical finding associated with severe holoprosencephaly.

A

Cyclopia (p.409)

22
Q

Name two posterior fossa malformations.

A

Chiari II (Arnold Chiari malformation); Dandy-Walker malformation (p.409)