SDL: Neuroembryology Flashcards

1
Q

what does the midline axial mesoderm form from?

A

the notochord

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2
Q

what does the notochord induce?

A

the overlying ectoderm, to form the neural plate

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3
Q

what is the difference between primary and secondary neurulation?

A

primary: developing notochord induces the overlying embryonic ectoderm to thicken and form the neural plate– secondary: coalescence of caudal mass mesenchymal cells into a rod followed by cavitation to form a tube and fusion with primary neural tube

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4
Q

in which process (primary or secondary neurulation) does the notochord play a role?

A

primary neurulation: notochord induces the overlying embryonic ectoderm to thicken and form the neural plate

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5
Q

what embryonic germ cell layer forms from the neural tube in primary and secondary neurulation?

A

primary: ectoderm fusion; secondary: mesenchymal condensation, epithelial translocation

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6
Q

what structures related to the PNS do neural crest cells give rise to?

A

spinal nerve ganglia, cranial nerve ganglia, ANS ganglia, schwann cells

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7
Q

what is the specific timing difference between closure of the anterior and posterior neuropores? which occurs last?

A

anterior neuropore closes on day 25; posterior neuropore closes on day 27

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8
Q

the 2 types of spina bifida

A

closed skin (occulta), open skin condition (neural plate is directly exposed to amniotic fluid)

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9
Q

spina bifida occulta typically occurs where? this is an example of what type of neurulation defect?

A

lumbar/upper sacral junction; secondary neurulation defect

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10
Q

if spina bifida occulta occurs in the upper regions of the vertebral column, it would arise from incomplete fusion of post. neuropore during..

A

primary neurulation (this is rare)

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11
Q

what is the difference between spina bifida occulta versus a meningocele versus a myelomeningocele? which would cause more severe neurological symptoms?

A

occulta: defect in vertebral arches, doesn’t involve neural tissue (no symptoms); meningocele: fluid-filled sac of meninges pokes through defect (Neuro symptoms); myelomeningocele: neural tissue in the fluid sac (neuro symptoms)

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12
Q

5 neural tube defects that are examples of primary neurulation defects

A

craniorachischisis totalis, anencephaly, myeloscisis, encephalocele and myelomeningocele

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13
Q

what would you call a defect where primary neurulation failed to occur anywhere in the fetus?

A

craniorachischisis totalis?

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14
Q

what would you call a defect where the ant neuropore failed to close in the region overlying the top of the head? what happens to the neural plate that is located in this region?

A

anencephaly; exposed neural tissue dies

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15
Q

what would you call a defect where there is an outpocketing of neural tissue in an instance where there is a partial failure of closure of the anterior neuropore in the region of the back of the head?

A

encephalocele

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16
Q

what would you call a defect in which there is complete failure to close the post neuropore?

A

myeloschisis

17
Q

what risk factors are there for neural tube defects? how can a pregnant mother reduce the risk of having a baby with a neural tube defect?

A

folic acid deficiency (sexually active women should take folic acid 2 mos before conception and throughout pregnancy), diabetic mothers, alcoholics, nutritional deficiencies

18
Q

which protein would increase in maternal serum and amniotic fluid in cases of neural tube defect?

A

alpha-fetal protein

19
Q

when should women of childbearing age begin taking daily supplements of folic acid? why?

A

2 mos before conception and throughout pregnancy to prevent neural tube defects

20
Q

what are the molecular mechanisms of neurulation? (will only be tested on sonic, bone morogenic protein, homeobox genes)

A

notochord secretes hedgehog protein that induces overlying ectoderm to differentiate into neuroectoderm; opposing sonic hedgehog bone morphogenic protein gradients promote the dorsoventral differentiation; spatial and temporal differences in the homeobox genes are important for anterior-posterior axis development and secondary neurulation

21
Q

which cells give rise to neuroblasts in the developing spinal cord?

A

neural crest cells in the cerebral cortex

22
Q

which cells give rise to the astrocytes and oligodendroglia?

A

neuroepithelial cells

23
Q

what causes holoprosencephaly?

A

failure to form the two cerebral hemispheres- fails to cleave, remains fused as a single midline entityra

24
Q

what is the function of the radial glia in the developing cerebral cortex?

A

neurons migrate along them; also progenitor cells

25
Q

what is the difference between schizencephaly, lissencephaly, pachygyri or polygyri?

A

schizencephaly (cleft brain, paralysis, seizures); lissencephaly (smooth brain, few gyri); pachygyri (broad gyri, too few gyri); polygyri (small gyri)

26
Q

what is the underlying cause of schizencephaly, lissencephaly, pachygyri or polygyri?

A

disorders of migration

27
Q

which condition has an abnormal cleft in the brain?

A

schizencephaly

28
Q

which condition has a generalized absence of cerebral cortical gyri?

A

lissencephaly