Child Neuro Flashcards

1
Q

When does primary neurulation occur? What is it?

A

3-4 wks
formation of the brain and spinal cord exluding formation of the lower spinal cord. secondary neurulation: later events inovled in sacral spinal cord

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2
Q

\What is the most sever neural tube defect? What happens?

A

craniorachischisis. failure of primary neurulation, absence of overlying skeleton and dermal covering.
leads to spontaneous early abortion

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3
Q

What is anencephaly?

A

failure of anterior neural tube closure. absent forebrain and upper brainstem; present lower brainstem. Usually stillbirths; if not, death in a first few days of life

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4
Q

What is myelomeningocoele?

A

spina bifida. limited failure in posterior neural tube closure. see primitive nerual tube-like structure in the lumbosacral region. defects in axial skeleton and dermal covering; protrusion of a sac containing meninges, CSF, and spinal cord elements. varying degress of motor, sensory, and sphincter dysfunction.

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5
Q

What is myeloschisis?

A

complete failure of posterior nerual tube closure. spinal cord incomplete w/ absent vertebrae and dermal covering. usually stillborns

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6
Q

What is spina bifida occulta?

A

weakness but no apparent problem

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7
Q

what is an meningocele?

A

just a protrusion of CSF in lumbosaccral region- no cord material

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8
Q

What is primary prevetion for neural tube defects?

A

folate supplementation prior to conception

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9
Q

When does prosencephalic development peak?

A

2-3 mo. gestation

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10
Q

What are key events of prosencephalic development?

A

formation at rostral end of neural tube after anterior neural tube closure. then,horizonal cleave to form optic veicles, olfactory bults, olfactory tracts; transverse cleavage form telencephalon and diencephalon, saggital cleave to form cerebral hemispheres, basal ganglia, lateral ventricles
then midline devo: corpus callosum septum pellucidu, optic chiasm, hypothalamus

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11
Q

What is one clue about the degree of prosencephalic problems?

A

degree of facial abnormalities

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12
Q

What is aprosencephaly?

A

failure of prosencephalic formation. absent telencephalon and diencephalon with a primitive brainstem. they have an overlying skeleton and dermal covering, so NOT anencephaly. infants still born or die in early infancy

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13
Q

What is holoprosencephaly? Spectrum?

A

failure of prosencephalic cleavage. may be alobar, or lobar

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14
Q

What are some features of holoprosencephaly?

A

absence of olfactory bulbs and tracts, single optic nerve and single median eye, hypotelorism, rudimentary nasal structure, single central incisor

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15
Q

What happens with agenesis of corpus callosum?

A

disorder of midline prosencephalic development affecting the commissural plate. red flag for other neuronal migration problems, but usually asymptomatic if occurring in isolation

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16
Q

When does neuronal prolif occur?

A

3-4 months gestation

17
Q

Key events of neuronal prolif?

A

symmetrical divisions: determine number of prolif. units
assymmetrical division: determine size of prolif units
generation of radial glia and glial multiplication

18
Q

What is micrencephaly?

A

decreased number or size of neuronal columns. with radial microbrain death is early, but in other cases may take a long time for intellectual disability to become apparent. risk factors: irradiation, maternal alcoholism, hyperphenylalaninemia, rubella, cocaine, genetics

19
Q

When does neuronal migration occur?

A

3-5 mo. gestation

20
Q

What are three key events of neuronal migration?

A

radial migration in the cerebru, in the cerebellu, and tangential migration in the cerebellum

21
Q

What is schizencephaly?

A

restricted or regional agenesis of germanative zones- wedgeshaped cleft lined by abnormal gray matter. CMV is a risk factor

22
Q

What is lissencephaly?

A

smooth brain: paucity of gyri and cortical organizational aberrations.