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

被引:67
作者
Evidente, VGH
Advincula, J
Esteban, R
Pasco, P
Alfon, JA
Natividad, FF
Cuanang, J
San Luis, A
Gwinn-Hardy, K
Hardy, J
Hernandez, D
Singleton, A
机构
[1] Mayo Clin, Dept Neurol, Scottsdale, AZ 85259 USA
[2] St Lukes Hosp, Inst Neurosci, Quezon City, Philippines
[3] Western Visayas State Univ, Med Ctr, Iloilo, Philippines
[4] Philippine Gen Hosp, Dept Neurol, Manila, Philippines
[5] St Lukes Hosp, Res & Biotechnol Div, Quezon City, Philippines
[6] Univ E Ramon Magsaysay, Mem Med Ctr, Quezon City, Philippines
[7] NIH, Bethesda, MD 20892 USA
关键词
dystonia; Lubag; XDP; parkinsonism;
D O I
10.1002/mds.10271
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
X-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 I I 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. (C) 2002 Movement Disorder Society.
引用
收藏
页码:1271 / 1277
页数:7
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