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The unique phenomenology of sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag")
Article de En | WPRIM | ID: wpr-633151
Bibliothèque responsable: WPRO
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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Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pénétrance / Syndromes parkinsoniens / Troubles dystoniques / Maladies génétiques liées au chromosome X / Dystonie / Dystonie musculaire déformante / Iles Type d'étude: Qualitative_research Limites du sujet: Adult / Aged / Female / Humans / Male langue: En Texte intégral: Philippine Journal of Neurology Année: 2012 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pénétrance / Syndromes parkinsoniens / Troubles dystoniques / Maladies génétiques liées au chromosome X / Dystonie / Dystonie musculaire déformante / Iles Type d'étude: Qualitative_research Limites du sujet: Adult / Aged / Female / Humans / Male langue: En Texte intégral: Philippine Journal of Neurology Année: 2012 Type: Article