Huntington's disease is best described as which of the following?

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Multiple Choice

Huntington's disease is best described as which of the following?

Explanation:
Huntington's disease is a genetic neurodegenerative disorder inherited in an autosomal dominant pattern. A mutation in the HTT gene causes a progressive loss of neurons in the basal ganglia and cortex, leading to increasingly abnormal movements, cognitive decline, and psychiatric changes. The key takeaway is that it’s a hereditary, dominant condition that produces progressive brain deterioration. The other descriptions don’t fit: it’s not a metabolic liver disorder, not an autoimmune disease at the neuromuscular junction, and not a contagious brain infection. Onset is typically in adulthood (often in the 30s–40s), though juvenile cases can occur.

Huntington's disease is a genetic neurodegenerative disorder inherited in an autosomal dominant pattern. A mutation in the HTT gene causes a progressive loss of neurons in the basal ganglia and cortex, leading to increasingly abnormal movements, cognitive decline, and psychiatric changes. The key takeaway is that it’s a hereditary, dominant condition that produces progressive brain deterioration. The other descriptions don’t fit: it’s not a metabolic liver disorder, not an autoimmune disease at the neuromuscular junction, and not a contagious brain infection. Onset is typically in adulthood (often in the 30s–40s), though juvenile cases can occur.

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