| Literature DB >> 24356267 |
Sergio A Rodríguez-Quiroga1, Dolores González-Morón, Tomoko Arakaki, Nélida Garreto, Marcelo A Kauffman.
Abstract
Machado-Joseph disease (MJD) is the most frequent dominantly inherited spinocerebellar ataxia. A marked phenotypic variability is a characteristic of this disorder that could involve non-cerebellar presentations. Based on several case reports describing pyramidal dysfunction as the main symptom at onset, a clinical form resembling hereditary spastic paraplegia has been proposed. We report here two further cases of MJD patients whose initial clinical presentation suggested hereditary spastic paraplegia, and a summary of the main findings of previously similar published reports. Our findings lent support to the proposal of a MJD subtype distinguished by a marked pyramidal dysfunction at onset, simulating a clinical picture of hereditary spastic paraplegia.Entities:
Keywords: Machado Joseph disease; SCA-3; ataxia; genetics; hereditary spastic paraplegia
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Year: 2013 PMID: 24356267
Source DB: PubMed Journal: Medicina (B Aires) ISSN: 0025-7680 Impact factor: 0.653