Congenital Diseases Flashcards

1
Q

How the Nervous System Develops From The First Few Days of Gestation?

A
  1. Neuroectodermal cells form the neural plate
  2. Neural Groove forms
  3. Groove closes to form Neural Tube
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2
Q

Primary Divisions of Neural Tube

A
  1. Forms the central nervous system
  2. Prosencephalon (forebrain)- Secondary divisions are telencephalon and diencephalon
  3. Mesencephalon (midbrain)
  4. Rhombencephalon (hindbrain)–secondary divisions are metencephalon and myelencephalon
  5. myelon
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3
Q

Enlarged head due to brain filled with water. What condition is this?

A

Hydranencephaly

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4
Q

Enlarged Head due to an abnormal increase of CSF.

A

Hydrocephalus

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5
Q

The general term of the enlarged head.

A

Macrocephaly

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6
Q

Secondary to cerebral disease and forms a small head. What condition is this associated?

A

Microcephaly

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7
Q

Failure of neural tube to close. What condition is this associated?

A

Rachischisis

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8
Q

Premature Closure of Cranial Sutures

A

Craniostenoses

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9
Q

Head is wide and short.

A

Brachycephalic- coronal suture

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10
Q

Head is long and thin.

A

Scaphocephalic- sagittal suture

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11
Q

Tower Skull

A

Oxycephalic- 2 sutures combined

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12
Q

What diagnostic tool should help to diagnose craniostenoses?

A

X-ray

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13
Q
  1. No scalp, skull, cortex, only white matter
  2. Telencephalon did not develop
  3. Pt donotsurvive more than 24 hrs
A

Anencephaly

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14
Q
  1. Gyri are absent
  2. Telencephalon did not develop
A

Lissencephaly

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15
Q
  1. One cerebral hemisphere only
  2. Prosencephaly didn’t divide into two
A

Holoprosencephaly

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16
Q
  1. Tubular Dilatation of the Spinal Cord
  2. May originate as expansion of central canal
  3. Weakness &sensory loss of upper ex
  4. Spastic Paraparesis is a late manifestation
A

Syringomyelia

17
Q

Disorders of fusion of the dorsal midline structures of neural tube

A

Rachishisis (Dysraphism)

18
Q

Types of Dysraphism

A
  1. Spina Bifida Occulta & Cystica
  2. Meningoencephalocele
  3. Arnold Chiari Malformation
  4. DandyWalker Syndrome
19
Q
  1. Incomplete closure of spinal vertebrae lamina
  2. No cyst, meninges stay inside spinal canal
  3. Adimple w/atuft of hair
  4. Detected radiologically
A

Spina Bifida Occulta

20
Q

Meninges come out and CSF form a cyst

A

Spina Bifida Cystica

21
Q

Only CSF in the cyst

A

Meningocele

22
Q

Includes spinal cord & roots

A

Myelomeningocele

23
Q

Frontal & Occipital affectation and CSF affected

A

Cranial Meningocele

24
Q

Frontal & Occipital affectation with CSF & Brain Tissue Affectation

A

Cranial Encephalocele

25
Q

`1. Downwarddisplacement of cerebellar tonsils, vermis, & medulla
2. Located in cerebellopontine and cervical spinal cord area

A

Arnold Chiari Malformation

26
Q

Cerebello-Medullary malformation alone of Arnold Chiari Malformation

A

Type 1

27
Q

Cerebello-Medullary malformation & spinal meningomyelocele of Arnold Chiari Malformation

A

Type 2

28
Q

Cerebello-Medullary malformation & occipital encephalocele of Arnold Chiari Malformation

A

Type 3

29
Q

Cerebellar Hypoplasia (Dandy-Walker) of Arnold Chiari Malformation

A

Type 4

30
Q

The 4th ventricle cyst & cerebellar vermis hypoplasia. Failure of development of midline cerebellum.

A

Dandy-Walker Syndrome

31
Q

Signs & Symptoms (Chiari Malformation)

A
  1. Signs of progressive hydrocephalus
  2. Cerebellar Ataxia
32
Q

Cyst at the Sylvian fissure, temporal area. Mostly asymptomatic but may present with focal signs

A

Arachnoid Cysts