Huntington’s Disease: A Comprehensive Analysis
Huntington's disease (HD) is a rare, autosomal dominant neurodegenerative disorder caused by a mutation in the HTT gene. This condition results in the progressive degeneration of neurons, predominantly in the striatum and cortex, manifesting in motor, cognitive, and psychiatric disturbances. Understanding the multifaceted nature of Huntington’s disease is crucial for developing more effective interventions and enhancing patient care.
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