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一例罕见的肢体带型肌营养不良症合并线粒体肌病病例。

An unusual case of muscular limb-girdle dystrophy and mitochondrial myopathy.

作者信息

Calore E E, Cavaliere M J, Wakamatsu A, Perez N M, Maeda M Y, Russo D H

机构信息

Instituto de Infectologia Emilio Ribas, Faculdade de Medicina da Universidade de São Paulo, Departemento de Patologia.

出版信息

Pathologica. 1994 Dec;86(6):649-51.

PMID:7617396
Abstract

Limb-girdle muscular weakness and wasting could be caused by different diseases (inflammatory and hereditary myopathies, muscular dystrophies and neurogenic atrophies). Among these, Limb-Girdle Muscular Dystrophy (LGMD) is an heterogeneous group of pathologies that have progressive proximal limbs and girdle weakness, with some dystrophic features by the muscle biopsy. We studied a case of LGMD in an adult man with a typical histological and histochemical profile, associated to a mitochondrial deficit characterized by presence of ragged-red fibers, a histochemical Cytochrome Oxidase deficiency and abnormal mitochondria by ultrastructure.

摘要

肢带型肌无力和萎缩可能由不同疾病引起(炎症性和遗传性肌病、肌肉营养不良症和神经源性萎缩)。其中,肢带型肌营养不良症(LGMD)是一组异质性疾病,具有进行性近端肢体和带肌无力,肌肉活检有一些营养不良特征。我们研究了一例成年男性LGMD病例,其具有典型的组织学和组织化学特征,并伴有线粒体缺陷,表现为存在破碎红纤维、组织化学细胞色素氧化酶缺乏以及超微结构下线粒体异常。

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