Other Basal Nuclei Disorders Flashcards

1
Q

Huntington’s Disease aka?

A

Huntington’s Chorea

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2
Q

What is Huntington’s disease?

A

an inherited neurodegenerative disease

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3
Q

What is wrong with the gene called Huntingtin?

A

there is an autosomal dominant mutation in either of the individual’s two copies

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4
Q

Children of Huntington’s disease pts have ___ risk of developing the disease also?

A

50%

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5
Q

What is the pathology of Huntington’s Disease?

A

gross atrophy of the striatum (caudate and putamen)

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6
Q

What is Huntington’s characterized by?

A

Triad of manifestations

  • Motor changes (choreoathetosis)
  • Cognitive decline leading to dementia
  • psychiatric disorders inclusing paranoia and psychosis behaviors
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7
Q

What is the typical age of onset for Huntington’s?

A

40-50 and most people progress to a vegetative state within 10-15 years and die

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8
Q

With Huntington’s there is an overall loss of GABAergic neurons and a reduction of what in the circuitry?

A

reduction of inhibition in the basal ganglia circuitry

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9
Q

in Huntington’s what happens to the subthalamic nuclei?

A

there is a loss of excitation of the subthalamic nucleus of the indirect pathway to the basal ganglia output nuclei

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10
Q

What approaches have been done to try and help Huntington’s?

A
  • dopamine ANTagonists
  • fetal transplantation (unsuccessful)
  • deep brain stimulation
  • surgical ablation of the GPi
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11
Q

What is hemiballismus?

A

wild, unpatterned, flinging movements of an entire extremity

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12
Q

what is hemiballismus caused by?

A

discrete lesion of the subthalamic nucleus contralateral to symptoms

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13
Q

pathology of hemiballismus?

A

reduces activity of the indirect pathway and thus reduces the inhibition of movement

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14
Q

what does hemiballismus most commonly result from?

A

vascular disorder of penetrating branch of posterior cerebral artery (PCA)

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