S4: Cerebellum & Ataxia Flashcards

(40 cards)

1
Q

The Cerebellum is Divided Anatomically into …..

A
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2
Q

The Cerebellum is Divided Histologically into …..

A
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3
Q

The Cerebellum is Divided Phylogenetically into …..

A
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4
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

A
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5
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

  • Consists of ….
A
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6
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

  • Phylogenitically
A
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7
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

  • Connected With
A
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8
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

  • Function
A
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9
Q

Compare Between Archi-Cerebellum & Paleo-Cerebellum & Neo-Cerebellum

  • Dysfunction
A
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10
Q

What are cerebellar syndromes?

A
  • Archi-Cereberallar Syndrome
  • Neo-Cerebellar syndrome
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11
Q

CP of Archi-Cerebellar Syndrome

A
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12
Q

CP of Neo-Cerebellar Syndrome

A
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13
Q

CP of Neo-Cerebellar Syndrome

  • Disturbance of Integration of voluntary moter characterized by ….
A
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14
Q

CP of Neo-Cerebellar Syndrome

  • Disturbance of compound movement:
A
  • Asthenia (Usually subjective).
  • Hypermetria and Hypometria.
  • Decomposition of movement.
  • Adiadochokinesia: Disturbance in patient’s ability to perform rapid alternative movements.
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15
Q

CP of Neo-Cerebellar Syndrome

  • Disturbance of muscle tone:
A

Hypotonia

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16
Q

Def of Ataxia

A
  • Incoordination of voluntary motor activity with or without disequilibrium in absence of
    motor weakness.
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17
Q

Types of Ataxia

A

1) Cerebellar ataxia.
2) Sensory ataxia.
3) Vestibular ataxia.
4) Combined ataxia.
5) Hysterical ataxia.

18
Q

Causes of Cerebellar Ataxia

A
  • Heredofamilial (i.e. hereditary ataxia)
  • Symptomatic
19
Q

Causes of Cerebellar Ataxia

  • Heredofamilial
A

Heredofamilial (i.e. hereditary ataxia)

  • Friedreich’s ataxia.
  • Marie’s ataxia.
20
Q

Causes of Cerebellar Ataxia

  • Symptomatic
21
Q

Def of Heredofamilial Ataxias

22
Q

Site of degeneration in Friedrich’s Ataxia

A
  • Spino-cerebellum.
  • Posterior column.
  • Pyramidal tract.
  • Peripheral nerves.
23
Q

Age in Friedrich’s Ataxia

A

The 1st decade.

24
Q

Onset in Friedrich’s Ataxia

25
Course in **Friedrich's Ataxia**
Slowly progressive.
26
CP in **Friedrich's Ataxia**
27
**Friedrich's Ataxia** is associated with .....
28
Sites of Degeneration in **Marie's Ataxia**
- Olive, Pontine nuclei. - Neo-cerebellum.
29
Age in **Marie's Ataxia**
The 2nd and 3rd decades.
30
Onset of **Marie's Ataxia**
Gradual
31
Course of **Marie's Ataxia**
Slowly Progressive
32
CP of **Marie's Ataxia**
1. Neo-cerebellar syndrome. 2. Preservation of deep reflexes. 3. Extensor planter response.
33
**Marie's Ataxia** is associated with
1. Ocular nerve palsies. 2. Mental impairment. 3. Extra-pyramidal syndromes.
34
INVx for **Heredofamilial Ataxia**
35
INVx for **Heredofamilial Ataxia** - Non-Structural INVx
- deficiency diseases, metabolic disorders, genetic...etc.
36
INVx for **Heredofamilial Ataxia** - Structural INVx
**Brain CT:** * Cerebellar hematoma, Large mass. **Brain MRI:** * Demyelination, Infarction, Congenital... etc.
37
TTT of **Heredofamilial Ataxia**
1. Physiotherary → For balance training. 2. Specific treatments → In cases of well-known treatable causes. 3. No specific pharmacotherapy → For hereditary ataxias.
38
Def of **Sensory Ataxia**
- It is due to interruption of the sensory pathways transmitting proprioceptive sensations.
39
Causes of **Sensory Ataxia**
40
Causes of **Vestibular-Labyrinthine Ataxia**
1. Menier's syndrome. 2. Labyrinthitis: viral or toxic. 3. Acoustic neuroma.