我们目前的3个家庭与该指数的影响音乐家病人的肌张力障碍，但其他形式的上肢重点任务的具体性肌张力障碍（ FTSD ） ，主要是书写痉挛，在7个亲人。我们的实验结果表明遗传贡献FTSD与表型变异，包括音乐家的肌张力障碍。
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...肌张力障碍(hereditaryprogressive dystonia with marked diurnal fluctuation,HPD)",是一种常染色体显性遗传的姿势性肌张力障碍(postural dystonia),其临床特征是症状...
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局限性肌张力障碍 focal dystonia
多巴反应性肌张力障碍 DRD ; dopa-reactivedystonia ; Dopa-Responsive Dystonia ; Dopamine-Responsive Dystonia
急性肌张力障碍 acute dystonia
畸形性肌张力障碍 dystonia musculorum deformans
变形性肌张力障碍 dystonia musculorum deformans ; dystonia musculorum deformans Chinese
原发性肌张力障碍 primary dystonia ; idiopathic torsion dystonia ; ITD
迟发性肌张力障碍 Tardive dystonia ; TDT
全身性肌张力障碍 generalized dystonia
节段性肌张力障碍 segmental dystonia
笔者通过对来自5个家庭7例多巴反应性肌张力障碍患者的护理。
Objective To attach importance to the nursing of dopa- responsive dystonia. Methods 7 cases from 5 families were treated and nursed with Dopa- therapy.
结论多巴反应性肌张力障碍临床表现呈多样化，临床表现与年龄密切相关。
Conclusion the clinical manifestations of DRD are various and they are closely correlated with age.
方法回顾性分析10例多巴反应性肌张力障碍患者的临床表现、诊断方法和治疗效果。
Methods Systematic study of clinical features, diagnosis and therapeutic effect in 10 patients with DRD was performed and retrospectively analyzed.
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