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Mov Disord ; 22(12): 1790-3, 2007 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-17579361

RESUMO

"Lubag" or X-linked dystonia-parkinsonism (XDP) is a genetic syndrome afflicting Filipino men. Intracranial surgical procedures for Lubag have been unsuccessful. We report a 45-year-old Filipino male with genetically confirmed XDP who underwent bilateral pallidal deep brain stimulation (DBS) surgery. The patient started to exhibit improvement on initial programming, most notably of his severe jaw-opening dystonia. At 1-year follow-up, his Burke-Fahn-Marsden dystonia score and motor Unified Parkinson's Disease Rating Scale score were improved by 71% and 62%, respectively, with the stimulators on compared to stimulators off state. Bilateral pallidal DBS may be a viable option for Lubag patients with medically refractory symptoms.


Assuntos
Terapia por Estimulação Elétrica , Doenças Genéticas Ligadas ao Cromossomo X/terapia , Globo Pálido/fisiopatologia , Doença de Parkinson/genética , Doença de Parkinson/terapia , Doenças Genéticas Ligadas ao Cromossomo X/patologia , Globo Pálido/efeitos da radiação , Humanos , Masculino , Pessoa de Meia-Idade , Doença de Parkinson/patologia
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