2 - Embryology of the Nervous System Flashcards

1
Q

How does the neural tube form?

A
  • 3rd week gastrulation produces notochord in mesoderm
  • Notochord sends signals to overlying ectoderm to differentiate to form neuroectoderm
  • The neural plate thickens and the lateral edges elevate and come together to form tube
  • Neural crest cells are released during this
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2
Q

What issues can arise during neural tube closure?

A
  • Neural tube fuses in the middle first and then the cranial and caudal ends close. If it doesn’t close then nerual tube defects
  • Occurs early in pregnancy
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3
Q

What is anencephaly?

A
  • Absence of a major portion of the brain, skull, and scalp that occurs due to the anterior neuropore not closing
  • Incompatible with life
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4
Q

What is Rachischisis?

A
  • Failure of the neuro folds to elevate so the neural tube doesn’t form so just flat primitive nervous tissue
  • Incompatible with life
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5
Q

How can we detect neural tube defects in utero and how do we prevent these from occuring?

A
  • Measure for raised alpha fetoprotein in the mother’s blood as this can leak from neural tube into amniotic fluid
  • Ultrasound
  • Take folic acid supplements three months before conception and throughout first trimester, as this helps epithelial folds to fuse together
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6
Q

What is spina bifida and the different types?

A
  • Usually at L5/S1 level and is due to the neural tube not fully closing so spinal cord issues and vertebral arches fail to fuse

- Occult: no protrusion or lumps, only missing vertebral arch

- Meningocele: meninges herniate through posterior vertebral arch defect but cord still in tact

- Myelomeningocele: meninges, CSF, bones, cartilage and spinal cord herniate through the defect and have neurological consequences

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7
Q

How does the spinal cord develop embryologically?

A
  • Most of the neural tube is the spinal cord. At first the cord grows at the same rate as the vertebral column but at third month column grows faster.
  • Therefore spinal roots have to elongate to exit at their intervetebral foramen, forming the cauda equina at L1
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8
Q

How does the brain form embryologically?

A
  • At the top of the neural tube 3 dilations form: forebrain (prosencephalon), midbrain (mesencephalon) and hindbrain (rhombencephalon)
  • Neural tube closes in 4th week and these are the three primary brain vesicles
  • 3 turn to 5 secondary vesicles at 5 weeks
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9
Q

What are the flexures that form during the embryological development of the brain?

A
  • Folds to fit

- Cephalic flexure: bend in the midbrain

- Cervical flexure: bend at the hindbrain-spinal cord junction

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10
Q

How does the ventricular system from embryologically?

A

Starts as lumen of the neural tube, CSF coming from the choroid plexus cells. Mainly draining back into the superior sagittal sinus or 1/3 apertures (2 lateral and 1 medial)

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11
Q

What is hydrocephalus and how is it treated?

A
  • Build up of CSF in the ventricles which can increase pressure in the skull leading to midline shift or compression symptoms
  • Blockage can be by stenosis, tumour, infection. Mainly in spina bifida children
  • Use ventricular peritoneal shunt, with length for growth, where shunt is connected to dilated ventricle so CSF reabsorbed into abdomen
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12
Q

What are the layers of the neural tube?

A
  • Tube lined by neuroectoderm layer
  • Intermediate layer of neuroblasts outside this and these develop into alar (sensory) and basal (motor) plate.
  • Plates divided by sulcus limitans and the outer marginal layer
  • Roof and floor plate help regulate organisation
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13
Q

In overview, what 5 things have to happen embryologically to form a nervous system?

A
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14
Q

Where do neural crest cells originate from?

A
  • Lateral border of the neuroectoderm tube
  • Get displaced and enter mesoderm and undergo EMT
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15
Q

What are some of the derivatives of neural crest cells?

A
  • Endocardial cushions
  • Dorsal root ganglion
  • Sympathetic ganglion
  • Schwann cells

Sensitive to alcohol, easily injured

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16
Q

Wht is Hirschsprung’s disease?

A
  • One structure affected by defect in neural crest cells, enteric ganglion leading to aganglionic megacolon
17
Q

What is DiGeorge syndrome?

A

Multiple structures affected by defect in neural crest cells, e.g thyrod deficiency, secondary immunodeficiency as no thymus, cardiac defects, abnromal face

18
Q

Answer the following SAQ.

A

A. Falx Cerebri

B. Right lower limb due to decussation and cortical homunculus

C. Superior and Inferior sagittal sinuses, anterior cerebral artery