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The diagnostic criteria of benign monomelic amyotrophy.

机译:良性单体肌萎缩症的诊断标准。

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I read the article entitled "Benign monomelic amyotrophy in a 7-year-old girl with proximal upper limb involvement: case report" with interest . I think that some of the diagnostic criteria for monomelic amyotrophy (MMA) suggested by the authors should be reviewed again. The authors stated that no familial patient has been presented to date. However, Gucuyener et al. reported two young siblings with MMA. They proposed that MMA, at least in that family, was inherited as an autosomal recessive trait. Nalini et al. also reported a familial case.
机译:我饶有兴趣地阅读了标题为“一名7岁上肢近端受累女孩的良性单核肌萎缩症:病例报告”的文章。我认为,作者提出的一些关于单体肌萎缩症(MMA)的诊断标准应再次进行审查。作者指出,迄今为止尚无家族性患者。但是,Gucuyener等。报告了两个年轻的MMA兄弟姐妹。他们提出,至少在该家族中,MMA是常染色体隐性遗传。 Nalini等。还报告了家族病例。

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