重症肌无力
脊髓性肌萎缩
医学
神经肌肉疾病
杜氏肌营养不良
肌营养不良
肌电图
中国人口
肌肉活检
儿科
人口
神经肌肉传递
内科学
活检
物理医学与康复
基因型
生物
疾病
遗传学
环境卫生
基因
作者
Brian Hon‐Yin Chung,Virginia Wong,Patrick Ip
标识
DOI:10.1177/08830738030180030201
摘要
Our objective was to study the prevalence of neuromuscular diseases in Chinese children. A prospective study of neuromuscular diseases in Chinese children was conducted from 1985 to 2001 in Hong Kong, which is a city in southern China. The population census of June 30, 2001, was used to calculate the prevalence of neuromuscular diseases in Chinese children. Altogether, 332 children aged < 19 years at first assessment with neuromuscular diseases confirmed by using electromyography, muscle biopsy, and/or molecular genetic study were included in the study. Of these, 228 (68%) had inherited and 104 (32%) had noninherited neuromuscular diseases. Of the inherited neuromuscular diseases, the most common were the dystrophinopathies, including Duchenne muscular dystrophy ( n = 66) and Becker muscular dystrophy ( n = 8). Spinal muscular atrophy was the second most common ( n = 61). Of the noninherited neuromuscular disorders, myasthenia gravis was the most common ( n = 62, 60%). Nearly 88% of the cases of myasthenia gravis were ocular type. The prevalence rate of neuromuscular diseases in June 2001 ( n= 291 surviving) is estimated to be 214 × 10 —6 . The estimated prevalence rate of neuromuscular diseases in our Chinese children is 1 in 4669. ( J Child Neurol 2003; 18: 217—219).
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