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迟发性肌肉磷酸果糖激酶缺乏症

Late-onset muscle phosphofructokinase deficiency.

作者信息

Danon M J, Servidei S, DiMauro S, Vora S

机构信息

Department of Neurology, University of Illinois College of Medicine, Chicago 60612.

出版信息

Neurology. 1988 Jun;38(6):956-60. doi: 10.1212/wnl.38.6.956.

Abstract

A 75-year-old man had a 10-year history of slowly progressive limb weakness without cramps or myoglobinuria. Clinical, morphologic, and biochemical studies showed muscle phosphofructokinase (PFK) deficiency. Erythrocyte PFK activity in his asymptomatic daughter was 63% of normal, compatible with a carrier state. The chronic myopathic variant of muscle PFK deficiency appears to be transmitted as an autosomal recessive trait and may be due to a distinct genetic defect.

摘要

一名75岁男性有10年缓慢进展的肢体无力病史,无痉挛或肌红蛋白尿。临床、形态学和生化研究显示肌肉磷酸果糖激酶(PFK)缺乏。他无症状女儿的红细胞PFK活性为正常的63%,符合携带者状态。肌肉PFK缺乏的慢性肌病变体似乎以常染色体隐性性状遗传,可能是由于一种独特的基因缺陷。

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