PSP‐Richardson 's Syndrome as a Rare Phenotypic Expression of Very Late‐Onset Huntington's Disease: A Case Report
Résumé
Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disease due to increased (≥36) CAG repeats in the first exon of the huntingtin gene (HTT). HD is classically characterized by generalized chorea, and slowly progressive parkinsonism and dystonia associated with psychiatric and cognitive disorders.1 However, very unusual presentations may also exist such as the one reported here.
Domaines
Neurobiologie
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Movement Disord Clin Pract - 2023 - Prange - PSP‐Richardson s Syndrome as a Rare Phenotypic Expression of Very Late‐Onset.pdf (401.68 Ko)
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