Neuro - Embryology Flashcards

Pg. 444-446 in First Aid 2014 Pg. 408-410 in First Aid 2013 Sections include: -Neural development -Regional specification of developing brain -CNS/PNS origins -Neural tube defects -Forebrain anomalies -Posterior fossa malformations -Syringomyelia -Tongue development

1
Q

What role does the notochord play in embryological development?

A

Notochord induces overlying ectoderm to differentiate into neuroectoderm and form the neural plate

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2
Q

To what does the neural plate give rise?

A

Neural plate gives rise to neural tube and neural crest cells

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3
Q

What is the fate of the notochord in adults?

A

Notochord becomes nucleus pulposus of the intervertebral disc in adults

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4
Q

During what time frame in embryogenesis does neural plate progress to neural tube and neural crest cells?

A

Day 18 - Day 21

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5
Q

What is the orientation of the alar versus basal plate? What are their functions?

A

Alar plate (dorsal): sensory; Basal plate (ventral): motor; Think: Same orientation as spinal cord

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6
Q

Draw a 3-stage progression of neurological development, labeling the following: (1) Neural plate (2) Notochord (3) Neural crest (4) Neural tube (5) Neural crest cells.

A

See p. 444 in First Aid 2014 or Pg. 408 in First Aid 2013 for image at top left

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7
Q

How many primary versus secondary vesicles are there in the developing brain? What are their names? Give 2 names for each of the primary vesicles.

A

3 PRIMARY VESICLES: (1) Forebrain (prosencephalon) (2) Midbrain (mesencephalon) (3) Hindbrain (rhombencephalon); 5 SECONDARY VESICLES: (1) Telencephalon (2) Diencephalon (3) mesencephalon (4) Metencephalon (5) Myelencephalon

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8
Q

To what secondary vesicles does the forebrain (prosencephalon) give rise? In turn, what adult brain structures develop from each of these secondary vesicles?

A

FOREBRAIN (PROSENCEPHALON) –> Telencephalon & Diencephalon; TELENCEPHALON –> Cerebral hemispheres (walls) & Lateral ventricles (cavities); DIENCEPHALON –> Thalamus (walls) & Third ventricle (cavities)

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9
Q

To what secondary vesicle does the midbrain (mesencephalon) give rise? In turn, what adult brain structures develop from this secondary vesicle?

A

MIDBRAIN (MESENCEPHALON) –> Mesencephalon; MESENCEPHALON –> Midbrain (walls) & Aqueduct (cavities)

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10
Q

To what secondary vesicles does the hindbrain (rhombencephalon) give rise? In turn, what adult brain structures develop from each of these secondary vesicles?

A

HINDBRAIN (RHOMBENCEPHALON) –> Metencephalon & Myelencephalon; METENCEPHALON –> Pons (walls), Cerebellum (walls), & Upper part of fourth ventricle (cavities); MYELENCEPHALON –> Medulla (walls) & Lower part of fourth ventricles (walls)

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11
Q

Draw and label the regional specification of the developing brain from primary vesicles to secondary vesicles to adult derivates (categorized as walls versus cavities derivatives).

A

See p. 444 in First Aid 2014 or Pg. 408 in First Aid 2013 for visual

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12
Q

Name 4 parts of the nervous system that are derived from neuroectoderm?

A

Neuroectoderm - (1) CNS neurons; (2) ependymal cells (inner lining of ventricles, make CSF); (3) oligodendroglia; (4) astrocytes

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13
Q

Name 2 parts of the nervous system that are derived from the neural crest?

A

Neural crest - (1) PNS neurons; (2) Schwann cells

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14
Q

Name one part of the nervous system that is derived from the mesoderm?

A

Mesoderm - Microglia; Think: “like Macrophages, originate from Mesoderm”

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15
Q

What happens if neuropores fail to fuse? At what week in development does this usually occur?

A

Neuropores fail to fuse (4th week) –> persistent connection between amniotic cavity and spinal canal

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16
Q

With what deficiency are neural tube defects associated, and in what context?

A

Associated with low folic acid intake before conception and during pregnancy.

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17
Q

What lab value may be elevated in neural tube defects, and from where is this measured?

A

Elevated alpha-fetoprotein (AFP) in amniotic fluid and maternal serum.

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18
Q

What is a helpful confirmatory test in neural tube defects, and why?

A

Increased acetylcholinesterase (AChE) in amniotic fluid is a helpful confirmatory test (fetal AChE in CSF transudates across defect into amniotic fluid).

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19
Q

Name 3 kinds of neural tube defects.

A

(1) Spina bifida occulta (2) Meningocele (3) Meningomyelocele

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20
Q

What happens (and does not happen) in spina bifida occulta?

A

Failure of bony spinal canal to close, but no structural herniation

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21
Q

Where is spina bifida occulta usually seen? What impact does it have on the integrity of the dura?

A

Usually seen at lower vertebral levels. Dura is intact.

22
Q

What are 2 physical findings with which spina bifida occulta is associated?

A

Associated with tuft of hair or skin dimple at level of bony defect.

23
Q

What happens (and does not happen) in meningocele?

A

Meninges (but not the spinal cord) herniate through spinal canal defect

24
Q

What happens in meningomyelocele?

A

Meninges and spinal cord herniate through spinal canal defect

25
Q

What are the AFP levels with meningocele like?

A

Normal AFP.

26
Q

Draw a vertebrate and skin depicting findings in each of the following situations: (1) Normal (2) Spina bifida occulta (3) Meningocele (4) Meningomyelocele. Be sure to include and label the following in your drawing: spinal cord, dura, leptomeninges, transverse process, and subarachnoid space.

A

See p. 445 in First Aid 2014 or p. 409 in First Aid 2013 for visual

27
Q

What causes anencephaly, and what results?

A

Malformation of anterior neural tube resulting in no forebrain, open calvarium (“frog-like appearance”)

28
Q

What are 2 clinical findings associated with anencephaly?

A

Clinical findings: increased AFP; Polyhydramnios (no swallowing center in brain)

29
Q

With what maternal condition is anencephaly associated?

A

Associated with maternal diabetes (type I).

30
Q

What intervention decreases risk of anencephaly?

A

Maternal folate supplementation decreases risk

31
Q

What event fails to occur in holoprosencephaly? When does this usually occur?

A

Failure of left and right hemispheres to separate; usually occurs during weeks 5-6.

32
Q

Briefly describe the etiology of holoprosencephaly. To what mutations may it be related?

A

Complex multifactorial etiology that may be related to mutations in sonic hedgehog signaling pathway

33
Q

What is the physical finding in moderate holoprosencepahly? What is the physical finding in its most severe form?

A

Moderate form has cleft lip/palate, most severe form results in cyclopia.

34
Q

Name 2 posterior fossa malformations.

A

(1) Chiari II (Arnold-Chiari malformation) (2) Dandy-Walker

35
Q

What is another name for Chairi II? What is it?

A

Arnold-Chiari malformation; Significant herniation of cerebellar tonsils and vermis through foramen magnum with aqueductal stenosis and hydrocephalus

36
Q

How does Chiari II often present?

A

Often presents with lumbosacral myelomeningocele and paralysis below the defect

37
Q

What defines Dandy-Walker?

A

Agenesis of cerebellar vermis with cystic enlargement of 4th ventricle (fills the enlarged poserior fossa)

38
Q

With what 2 other neurologic conditions is Dandy-Walker associated?

A

Associated with hydrocephalus & spina bifida.

39
Q

What does “Syrinx” mean? What defines syringomyelia? What happens if the central canal is involved?

A

Syrinx = tube (as in syringe); Cystic cavity (syrinx) within the spinal cord (if central canal –> hydromyelia)

40
Q

Which fibers are typically damaged first in syringomyelia? What neurological deficit results from syringomyelia? What related ability is preserved?

A

Crossing anterior spinal commissural fibers are typically damaged first; Results in a “cape-like,” bilateral loss of pain and temperature sensation in upper extremities (fine touch sensation is preserved)

41
Q

At what vertebral levels is syringomyelia most common?

A

Most common at C8-T1

42
Q

With what other neurological condition is syringomyelia associated? Define this condition and give its presentation in an adult versus child. Draw a visual depicting both this condition and syringomyelia.

A

Associated with Chiari I malformation (>3-5 mm cerebella tonsillar ectopia; congenital, usually asymptomatic in childhood, manifests with headaches and cerebellar symptoms); See p. 446 in First Aid 2014 or p. 410 in First Aid 2013 for visual

43
Q

What forms the anterior 2/3 of the tongue? What nerves provide sensation and taste for the anterior 2/3 of the tongue?

A

1st and 2nd branchial arches form anterior 2/3 (thus sensation via CN V3, taste via CN VII)

44
Q

What forms the posterior 1/3 of the tongue? What nerves provide sensation and taste for the posterior 1/3 of the tongue?

A

3rd and 4th branchial arches form posterior 1/3 (thus sensation and taste mainly via CN IX, extreme posterior via CN X)

45
Q

What nerve provides motor innvervation for the tongue?

A

Motor innervation is via CN XII

46
Q

From which myotomes are the muscles of tongue derived?

A

Muscles of the tongue are derived from occipital myotomes.

47
Q

Which cranial nerves allow the tongue to taste?

A

Taste - CN VII, IX, X (solitary nucleus)

48
Q

Which cranial nerves allow the tongue to perceive pain?

A

Pain - CN V3, IX, X

49
Q

What cranial nerve handles motor function of the tongue?

A

Motor - CN XII

50
Q

Draw the tongue and its parts, labeling each part’s innervation and embryologic origin.

A

See p. 446 in First Aid 2014 or p. 410 in First Aid 2013 for visual