Congenital Malformations Flashcards

1
Q

What types of defects are there? [9]

A
  • Failure of neural tube closure
  • CSF accumulation
  • Problems with Gyri Formation
  • Corpus Callosum
  • Head size
  • Cysts/cavities
  • Clefts/slits
  • Split cord
  • Intelluctual
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2
Q

List some abnormalities caused by failure of the neural tube [3]

A

Anencephaly (Ant neuropore doesnt close)

Encephalocoele (Rostral neural tube failure)

Spina Bifida (Caudal neuropore doesn’t close right leading to non-fused vertebral arches)

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3
Q

How does Anencephaly develop?

A

Anterior neuropore doesnt close so the skull doesnt form over the brain and (exposed to the outside) it degenerates –> Death

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4
Q

How does Encephalocoele develop?

A

The rostral neural tube fails causing a defect in the skull through which cerebral tissue herniates.
This can cause a varying degree of neurological deficits based on location and level of herniation

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5
Q

How does spina bifida develop?

A

Caudal neural tube fails to close properly so you end up with non-fused vertebral arches
(Often has herniation out the spinal column in the lower back)

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6
Q

What is the most minor form of spina bifida?

Clinical examination findings? [2]

A

Spina Bifida Occulta

This occurs in 10% of peoples L5/6 vertebrae with usually no clinical symptoms.
Sometimes it has a dimple with a tuft of hair there.

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7
Q

What are the types of protrusion through the defect in spina bifida? [3]

A

Collectively called Spina Bifida Cystica.

  • Spina Bifida with Meningocele (Protrusion of meninges & CSF)
  • Spinal Bifida with Meningomyelocle (Nerve roots/spinal cord also protrude causing loss of sensation and paralysis below lesion)
  • Myeloschisis (Spinal cord open due to failure of neural folds to fuse - Complete loss of function/sensation below the lesion causing lower limb paralysis and bladder problems)
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8
Q

How can we prevent neural tube malformations? [2]

A
  • Screening

- Folic Acid Supplements (Very important to neural tube for no apparent reason)

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9
Q

What screening methods are there for neural tube malformations? [3]

A

Maternal Blood Screening:

  • Raised Serum Alpha Fetoprotein
  • AFP from foetal liver leaks into amniotic fluid through open neural tube and into maternal blood

Amniocentesis:
- Raised AFP in amniotic fluid

Ultrasound:
- Anencephaly and Spina Bifida

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10
Q

What risk factors are there for neural tube malformations? [3]

A
  • Genetic Predisposition
  • Nutrional (e.g. too little folate or too much Vit A)
  • Environmental e.g. Hyperthermia or Drugs (e.g. Na Valproate)
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11
Q

What is Hydrocephalus?

A

CSF cant drain so it builds up resulting in an enlarged brain and cranium, usually due to blocked cerebral aqueduct.

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12
Q

What causes hydrocephalus? [4]

A
  • Genetic
  • Prenatal Viral Infection
  • Intraventricular Haemorrhage
  • Spina Bifida Cystica
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13
Q

What do we call it if the Gyri/Sulci fail to develop?

A

Lissencephaly or “smooth Brain”.

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14
Q

What causes Lissencephaly?

A

Defective Neuronal Migration

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15
Q

Sequelae of Lissencephaly? [4]

A
  • Severe Mental Impairment
  • Failure to Thrive
  • Seizures
  • Abnormal Muscle Tone

(Many die before 10)

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16
Q

Other than lissencephaly what conditions affect the gyri?

A

Polymicrogyria

An excessive number of small gyri with a variable degree of neurological problems

17
Q

What causes microcephaly [3] and how does it present [5] ?

A

Genetics, drugs and infection e.g. Zika

Intellectual impairment
Delayed Motor function/speech
Seizures
Balance/Co-ordination problems
Hyperactivity
18
Q

What congenital malformation affects the Corpus Callosum?

A

Agenesis of the Corpus Callosum (Partial or incomplete)

Effects range from subtle cognitive/social difficulties up to severe impairment, seizures and hypotonia etc

19
Q

What causes CSF filled Cysts or cavities? [1]

A

Porencephaly

Due to postnatal stroke or infection

20
Q

What causes Clefts or slits in the brain? [3]

A

Genetics, in utero stroke or infection.

Called Schizencephaly

21
Q

Define Diastematomyelia?

A

Spinal cord split longitudinally in two, associated with other vertebral anomalies.

Causes loss of sensation, weakness, scoliosis, hairy lower back and foot deformities.