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Phenomenology of "Lubag" or X-linked dystonia-parkinsonism

dc.contributor.authorEvidente, Virgilio Gerald
dc.contributor.authorAdvincula, Joel
dc.contributor.authorEsteban, Raymund
dc.contributor.authorPasco, Paul
dc.contributor.authorAlfon, Jhoe Anthony
dc.contributor.authorNatividad, Filipinas F.
dc.contributor.authorCuanang, Joven
dc.contributor.authorSan Luis, Amado
dc.contributor.authorGwinn-Hardy, Katrina
dc.contributor.authorHardy, John
dc.contributor.authorHernandez, Dena
dc.contributor.authorSingleton, Andrew
dc.coverage.spatialCapizen
dc.coverage.spatialPanayen
dc.date.accessioned2024-05-03T02:30:59Z
dc.date.available2024-05-03T02:30:59Z
dc.date.issued2002-06-24
dc.identifier.citationEvidente, V. G. H., Advincula, J., Esteban, R., Pasco, P., Alfon, J. A., Natividad, F. F., Cuanang, J., San Luis, A., Gwinn-Hardy, K., Hardy, J., Hernandez, D. & Singleton, A. (2002). Phenomenology of "Lubag" or X-linked dystonia-parkinsonism. Movement Disorders, 17(6), 1271-1277.en
dc.identifier.issn0885-3185
dc.identifier.urihttps://hdl.handle.net/20.500.14353/411
dc.description.abstractX-linked dystonia-parkinsonism (XDP), or Lubag syndrome, is known to cause progressive dystonia, with or without parkinsonism, among Filipino male adults with maternal roots from the Philippine island of Panay. We present cinematographic material of 11 cases of Lubag carrying the XDP haplotypes who manifest with a wide spectrum of movement disorders, including dystonia, tremor, parkinsonism, myoclonus, chorea, and myorhythmia. Because of overlapping features, Lubag patients are commonly misdiagnosed as idiopathic dystonia, essential tremor, Parkinson's disease, or Parkinson's-plus syndromes. Thus, it is imperative to elicit an exhaustive family history in any Filipino male adult who presents with a movement disorder.en
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.subjectDystoniaen
dc.subjectLubagen
dc.subjectParkinsonismen
dc.subjectXDPen
dc.subjectLubag syndromeen
dc.subjectMyoclonusen
dc.subjectChoreaen
dc.subjectMyorhythmiaen
dc.subjectIdiopathic dystoniaen
dc.subjectParkinson's-plus syndromesen
dc.subjectFamily historyen
dc.subject.lcshDystoniaen
dc.subject.lcshParkinson's diseaseen
dc.subject.lcshMovement disordersen
dc.subject.lcshPhenomenologyen
dc.subject.lcshSyndromesen
dc.subject.lcshFilipinosen
dc.subject.lcshPhenotypeen
dc.subject.lcshGenetic disordersen
dc.subject.lcshGenetic disorders--Diagnosisen
dc.subject.lcshGeneticsen
dc.subject.lcshHuman geneticsen
dc.subject.lcshMiddle-aged menen
dc.subject.lcshTremoren
dc.subject.lcshChoreaen
dc.subject.lcshGenealogyen
dc.subject.meshDiagnosis, Differentialen
dc.subject.meshDystonic Disordersen
dc.subject.meshGenetic Carrier Screeningen
dc.subject.meshGenetic Diseases, X-Linkeden
dc.subject.meshGenetic Markersen
dc.subject.meshHumansen
dc.subject.meshMaleen
dc.subject.meshNeurologic Examinationen
dc.subject.meshParkinsonian Disordersen
dc.subject.meshPhenotypeen
dc.subject.meshEthnologyen
dc.titlePhenomenology of "Lubag" or X-linked dystonia-parkinsonismen
dc.typeArticleen
dcterms.accessRightsLimited public accessen
dc.citation.journaltitleMovement Disordersen
dc.citation.volume17en
dc.citation.issue6en
dc.citation.firstpage1271en
dc.citation.lastpage1277en
dc.identifier.essn1531-8257
dc.identifier.doi10.1002/mds.10271
local.isIndexedByScopusen


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