Neuro5 Flashcards

Huntington's Disease Movement Disorders

1
Q

What type of disorder is Huntington’s dz?

A

Autosomal-Dominant
Trinucleotide repeat – CAG
Chromosome 4

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2
Q

When does the expansion of CAG repeats occur in Huntington’s?

A

Spermatogenesis

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3
Q

What is the cause of neuronal death in Huntington’s?

A

NMDA-R binding & Glutamate toxicity

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4
Q

What changes can be seen on imaging of Huntington’s?

A

Atrophy of Striatal Nuclei

- Main inhibitors of movement

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5
Q

What is the mnemonic for remembering Huntington’s Disease

A

CAG trinucleotide repeat:

“Caudate loses Ach & Gaba”

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6
Q

Movement Disorder: Hemiballismus

  • Presentation:
  • Lesion:
  • Notes:
A

Movement Disorder: Hemiballismus

  • Presentation:
  • Sudden, wild flailing of 1 arm +/- ipsilateral leg
  • Lesion:
  • Contralateral Subtahalmic nucleus (e.g., lacunar stroke)
  • Notes
  • Half-of-body ballistic” (contralateral lesion)
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7
Q

Movement Disorder: Chorea

  • Presentation:
  • Lesion:
  • Notes:
A

Movement Disorder: Chorea

  • Presentation:
  • Sudden, Jerky, Purposelsess movements
  • Lesion:
  • Basal ganglia (e.g., Huntington’s)
  • Notes
  • Chorea = dancing
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8
Q

Movement Disorder: Athetosis

  • Presentation:
  • Lesion:
  • Notes:
A

Movement Disorder: Athetosis

  • Presentation:
  • Slow, Writhing movements; especially seen in FINGERS
  • Lesion:
  • Basal Ganglia (e.g., Huntington’s)
  • Notes:
  • Writhing, snake-like movements
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9
Q

Movement Disorder: Myoclonus

  • Presentation:
  • Notes:
A

Movement Disorder: Myoclonus

  • Presentation:
  • Sudden, brief, uncontrolled muscle contraction
  • Notes:
  • Jerks; hiccups; common in METABOLIC abnormalities as Renal and Liver failure
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10
Q

Movement Disorder: Dystonia

  • Presentation:
  • Notes:
A

Movement Disorder: Dystonia

  • Presentation:
  • Sustained, involuntary muscle contractions
  • Notes:
  • Writer’s cramp; blepharospasm (sustained eyelid twitch)
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11
Q

Movement Disorder: Essential Tremor

  • Presentation:
  • Notes:
A

Movement Disorder: Essential Tremor

  • Presentation:
  • Action tremor; exacerbated by holding posture/limb position
  • Notes:
  • Genetic predisposition
  • Patients often self-medicate w/ EtOH
  • Tx: beta-blockers, primidone
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12
Q

Movement Disorder: Resting Tremor

  • Presentation:
  • Lesion:
  • Notes:
A

Movement Disorder: Resting Tremor

  • Presentation:
  • Uncontrolld movement of distal appendages (hands most noticeable)
  • Tremor alleviated by intentional movement
  • Lesion:
  • Parkinson’s disease
  • Notes:
  • Occurs at rest
  • “Pill-rolling tremor” of Parkinson’s
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13
Q

Movement Disorder: Intention Tremor

  • Presentation:
  • Lesion:
A

Movement Disorder: Intention Tremor

  • Presentation:
  • Slow, zig-zag motion when pointing/extending toward a target
  • Lesion:
  • Cerebellar dysfunction
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