Article Dans Une Revue Movement Disorders Clinical Practice Année : 2024

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.

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Neurobiologie
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hal-04801803 , version 1 (27-01-2025)

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Stéphane Prange, Chloé Laurencin, Pauline Roche, Isabelle Quadrio, Stéphane Thobois. PSP‐Richardson 's Syndrome as a Rare Phenotypic Expression of Very Late‐Onset Huntington's Disease: A Case Report. Movement Disorders Clinical Practice, 2024, 11 (3), pp.303-305. ⟨10.1002/mdc3.13943⟩. ⟨hal-04801803⟩
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