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ABSTRACT
Sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag") is an adult-onset, progressive, debilitating movement disorder first described in Filipino males from Panay Island in 1975. XDP manifests predominantly as torsion dystonia, later combined with or sometimes replaced with parkinsonism. Within the Island of Panay, the preva-lence rate is highest in the province of Capiz, where 1:4000 men suffer from the disorder. There is a high degree of penetrance and generalization. While women often serve as carriers, XDP is not limited to men. An updated XDP Philippine registry (as of January 2010) has identified 505 cases, with 500 males and 5 females. While some report that females may carry a milder form of the disorder, in our experience, both sexes generally follow a similar progressive clinical course.
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Full text: 1 Index: WPRIM Main subject: Penetrance / Parkinsonian Disorders / Dystonic Disorders / Genetic Diseases, X-Linked / Dystonia / Dystonia Musculorum Deformans / Islands Type of study: Qualitative_research Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Philippine Journal of Neurology Year: 2012 Type: Article
Full text: 1 Index: WPRIM Main subject: Penetrance / Parkinsonian Disorders / Dystonic Disorders / Genetic Diseases, X-Linked / Dystonia / Dystonia Musculorum Deformans / Islands Type of study: Qualitative_research Limits: Adult / Aged / Female / Humans / Male Language: En Journal: Philippine Journal of Neurology Year: 2012 Type: Article