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[麦卡德尔病]

[McArdle's disease].

作者信息

Lavrnić D V, Svetković D, Apostolski S, Rakocević-Stojanović V, Trikić R

机构信息

Department of Neurology, University Clinical Centre, Belgrade.

出版信息

Srp Arh Celok Lek. 1992 Jul-Aug;120(7-8):255-8.

PMID:1306014
Abstract

Glycogenosis type V (McArdle disease) is a serious metabolic disorder with an exercise intolerance, myalgia, early fatigue and stiffness of exercising muscles, relieved++ by rest. The authors present a case report of patient with McArdle's disease, and diagnostic procedures which can be used in different diagnostic of metabolic myopathies, especially between myoadenylate deaminase deficiency and different types of gly(geno)lytic myopathies. The importance of "ischemic forearm test" and muscle biopsy is emphasized.

摘要

糖原贮积病Ⅴ型(麦克尔迪病)是一种严重的代谢紊乱疾病,表现为运动不耐受、肌痛、运动肌肉早期疲劳和僵硬,休息后症状缓解。作者报告了一例麦克尔迪病患者的病例,并介绍了可用于不同类型代谢性肌病诊断的诊断程序,特别是在肌腺苷酸脱氨酶缺乏症和不同类型糖原分解性肌病之间的诊断。强调了“缺血性前臂试验”和肌肉活检的重要性。

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