Development of the Nervous System Flashcards

1
Q

nervous system develops from what embryonic layer

A

ectoderm

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2
Q

Neural tube gives rise to——

Brain in greek
Brain in latin

A

CNS (brain + spinal cord

Greek-encephalon
Latin-Cerebrum

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3
Q

Notochord embryonic origin

A

mesodermal origin,

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4
Q

Notochord development induces formation of

A

neural plate ( neural tube + neural crest)

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5
Q

what is primary neuralation

A

the process by which d neural folds fuse
forming a neural
tube.

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6
Q

derivatives of neural crest cells

A

● Pseudounipolar ganglion cells of the spinal and
cranial nerve ganglia
● Schwann cells (which elaborate the myelin sheath)
● Multipolar ganglion cells of autonomic ganglia.
● Leptomeninges (the pia-arachnoid), which envelop
the brain and spinal cord 5. Chromaffin cells of the
suprarenal medulla (which elaborate epinephrine).
● Pigment cells (melanocytes)
● Odontoblasts (which elaborate predentin)
● Aorticopulmonary septum of the heart
● Parafollicular cells (calcitonin-producing C-cells)
● Skeletal and connective tissue components of the
pharyngeal arches

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7
Q

neural crest cell gives rise to the PNS which consists of

A

● Peripheral
nerves
● Sensory ganglia
● Autonomic
ganglia

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8
Q

The alar plate of the brainstem & spinal cord gives rise to —– neurons

A

sensory neurons

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9
Q

The basal plate of the brainstem & spinal cord gives rise to —– neurons

A

motor neurons

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10
Q

protein in amniotic fluid which indicates neural tube defect

A

alpha-fetoprotein

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11
Q

3 main vesicles from neural tube

A

Forebrain (prosencephalon)
Midbrain (mesencephalon)
Hindbrain (Rhombencephalon)

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12
Q

cavity of Telencephalon
(cerebral hemispheres)

A

lateral ventricles

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13
Q

5 vesicles

A

Telencephalon
Diencephalon
Mesencephalon
Metencephalon
Myelencephalon

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14
Q

cavity of diencephalon (thalamus + optic vesicle)

A

Third ventricle

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15
Q

cavity of mesencephalon (Mid brain)

A

cerebral aqueduct

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16
Q

cavity of metencephalon (pons and cerebellum)

A

upper 4th ventricle

17
Q

cavity of Myelencephalon (medulla)

A

Lower 4th ventricle

18
Q

3 layers of the spinal cord

A

inner - ventricular layer
intermediate -mantle layer
outer- marginal layer

19
Q

layer that forms the white matter
of the SC

A

marginal Layer

20
Q

layer that forms the gray matter
of the Spinal cord

A

mantle layer

21
Q

End of the spinal cord is

A

Conus medullaris
L3- Children
L1- Adult

22
Q

Part of the brain derived from dorsal surface of alar plate

A

Cerebellum

23
Q

Anterior neuropore gives rise to —–
Failure to close

A

Lamina terminalis
Anencephaly : partial or complete absence of the brain with associated
defects of the cranial vault and scalp.

24
Q

Failure of posterior neuropore to close

A

spina bifida (myeloschisis)

25
Q

Anterior neuropore closes by Day
Posterior neuropore close by Day
Period of primary gastrulation

A

25
27
18-28

26
Q

Type of spina bifida,
there is no involvement of the
meninges or the underlying spinal
cord, and the overlying skin is
closed.

A

Spina bifida occulta ( defect of mesodermal origin)

27
Q

Spina bifida aperta with protrusion
○ of either the meninges alone is ———
○ spinal cord together with the meninges Is ——-

A

Meningocele
Meningomyelocele

28
Q

Protrusion of a sac from the cranium consisting of portions of
the meninges and CSF, glial tissue, and brain substance with or without the ventricles due to failure of anterior neuropore to close is

A

Encephalocele
-could be frontal or occipital encephalocele

29
Q

HYdrocephalus
(excess accu. of CSF In subarachnoid space &ventricles) is commonly caused by stenosis of

A

Cerebral aqueduct

30
Q

Dandy walker syndrome is Congenital absence of the —– and ——which through lack of communication with the remainder of the ventricular system,
can be one cause of hydrocephalus.

A

lateral apertures (of Luschka)
median aperture (of Magendie),

31
Q

Clinical manifestations of Dandy walker syndrome

A

Dandy-Walker Syndrome:
● Dilated fourth ventricle,
● Water on the brain,
● Small vermis

32
Q

What is arnold-chiari malformation

A

elongation and herniation of the cerebellar tonsils though the foramen magnum thereby blocking CSF flow

33
Q

Failure of midline cleavage of embryonic forebrain

A

Holoprosencephaly

( most severe manifestation of fetal alcohol syndrome)

34
Q

Defect in the occipital bone through which meninges, cerebellar tissue, and 4th ventricle may herniate

A

Cranium bifidum

35
Q

Obstructive hydrocephalus is due to

A
  • Dilated Lateral and III ventricles
  • Constriction of the Cerebral Aqueduct
36
Q

abnormal closure of anterior neuropore affecting the
midbrain, hindbrain and entire spinal region dev.

A

craniorachischisis,

37
Q

Anencephaly with defects confined to the midbrain

A

meroanencephaly

38
Q

Anencephaly with lesions extending into the hindbrain

A

Holoanencephaly

39
Q

NTD teratogen
Signalling req. for closure

A

Retinoid

PCP Signalling