Congenital muscular dystrophy

Conclusions Two types of CMD were present in our group. Merosin-deficient congenital muscular dystrophy ( congenital muscular dystrophy 1A, MDC1A) was more common, accompanied by abnormalities of the white matter.

结论本组CMD中merosin染色既有阴性，也有阳性，merosin缺乏症（先天性肌营养不良1A型）更为常见，伴随脑白质病变。

Aim: To study the clinicopathologic manifestation of a pedigree of autosomal dominant benign congenital muscular dystrophy ( BCMD).

目的：对一良性先天性肌营养不良家系进行临床分析及肌活检组织学观察。

I am16 years old and live in Ontario, Canada and have congenital muscular dystrophy.

我今年16岁，住在加拿大安大略省，患有先天性肌营养不良。

Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression

先天性肌营养不良的诊断及层黏连蛋白表达的意义

Members will recall that the sun moved juvenile yellow figures Ge& it? 7-year-old when he was diagnosed with congenital progressive muscular dystrophy.

大家还记得感动人物&阳光少年黄舸吗？他7岁时，被确诊为先天性进行性肌营养不良。

Results The results showed Duchenne muscular dystrophy in 15 cases, congenital muscular dystrophy in 1 case and congenital myopathy ( sarcotubular myopathy) in 1 case.

结果活检病理诊断假性肥大性肌营养不良15例，先天性肌营养不良1例，先天性肌病（肌质管病）1例。

Analysis of genotype and phenotype in Fukuyama congenital muscular dystrophy

福山型先天性肌营养不良基因型和表型分析

A pedigree study on benign congenital muscular dystrophy

良性先天性肌营养不良一家系研究