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Pharmacogenetics in the Treatment of Huntington’s Disease: Review and Future Perspectives

22 Feb 2023

Abstract excerpt

Huntington's disease (HD) is an autosomal dominant progressive brain disorder, caused by a pathological expansion of a CAG repeat that encodes the huntingtin gene. This genetic neurodegenerative rare disease is characterized by cognitive, motor, and neuropsychiatric manifestations. The aim of the treatment is symptomatic and addresses the hyperkinetic disorders (chorea, dystonia, myoclonus, tics, etc.) and the...

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PMID: 36983567
DOI: 10.3390/jpm13030385

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