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原发性肌阵挛性肌张力障碍:一种在儿童中常被漏诊的疾病。

Primary Myoclonus-Dystonia: A Diagnosis Often Missed in Children.

作者信息

Ghosh Debabrata, Indulkar Shalaka

机构信息

Supplementary material for this article is available on the Journal of Child Neurology website at http://jcn.sagepub.com/supplemental.

出版信息

J Child Neurol. 2013 Nov;28(11):1418-1422. doi: 10.1177/0883073813488677. Epub 2013 Jun 6.

Abstract

Primary myoclonus-dystonia is a childhood-onset autosomal-dominant movement disorder with myoclonic jerks and dystonia. The authors report 9 children (4 boys, 5 girls) with myoclonus-dystonia from 8 families seen over a 4-year period at Cleveland Clinic. The mean age of onset of symptoms was 2.8 years, but the diagnosis was made at a mean of 7.3 years. Myoclonus was the presenting symptom in 8 children. A known pathogenic mutation in the ε-sarcoglycan gene (SGCE) was identified in 4 of the 9 children, and 2 other children had novel mutations in the same gene. Good response to trihexyphenidyl and clonazepam was seen. Two patients underwent deep brain stimulation surgery of the bilateral globus pallidus pars interna. In 7 children, the diagnosis of myoclonus-dystonia was not considered by the referring child neurologists, which led to extensive investigations and a delay in the final diagnosis. In this report, the authors highlight the need for increased awareness of this entity among child neurologists.

摘要

原发性肌阵挛性肌张力障碍是一种起病于儿童期的常染色体显性遗传性运动障碍,伴有肌阵挛性抽搐和肌张力障碍。作者报告了在克利夫兰诊所4年期间接诊的来自8个家庭的9名患有肌阵挛性肌张力障碍的儿童(4名男孩,5名女孩)。症状出现的平均年龄为2.8岁,但确诊时的平均年龄为7.3岁。8名儿童以肌阵挛为首发症状。9名儿童中有4名被鉴定出ε-肌聚糖基因(SGCE)存在已知的致病突变,另外2名儿童在同一基因中有新的突变。观察到对苯海索和氯硝西泮反应良好。两名患者接受了双侧苍白球内侧部的脑深部电刺激手术。在7名儿童中,转诊的儿童神经科医生未考虑肌阵挛性肌张力障碍的诊断,这导致了广泛的检查以及最终诊断的延迟。在本报告中,作者强调儿童神经科医生需要提高对该疾病的认识。

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