Advances in diagnosis and treatment of limb-girdle muscular dystrophy

Meng Yu, Zhao-xia Wang
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引用次数: 0

Abstract

Limb - girdle muscular dystrophy (LGMD) is a group of disorders caused by gene mutations, with proximal muscle weakness as their main manifestation. Although various subtypes of LGMD share the common feature, heterogenity exist both in clinical phenotype and genetic defects. The diagnosis should be based on the combination of the clinical symptoms, muscle imaging findings, myo-pathological changes and genetic testing. Multi - discipline management is currently for patients. There has been progress in the diagnosis and treatment of LGMD worldwide in recent years. This review will summarize the advances in the LGMD diagnosis, treatment as well as clinical features of different subtypes of LGMD in order to improve the understanding of LGMD. DOI: 10.3969/j.issn.1672-6731.2017.08.005
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肢带肌营养不良的诊断和治疗进展
肢带型肌营养不良(LGMD)是一组由基因突变引起的疾病,其主要表现为近端肌无力。尽管LGMD的各种亚型具有共同的特征,但在临床表型和遗传缺陷方面都存在异质性。诊断应结合临床症状、肌肉影像学表现、肌肉病理变化和基因检测。多学科管理目前是为病人。近年来,世界各地在LGMD的诊断和治疗方面取得了进展。本文将综述LGMD的诊断、治疗进展以及不同亚型LGMD的临床特征,以提高对LGMD的认识。DOI:10.3969/j.issn.1672-6731017.08.005
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来源期刊
中国现代神经疾病杂志
中国现代神经疾病杂志 Medicine-Neurology (clinical)
CiteScore
0.40
自引率
0.00%
发文量
4914
审稿时长
10 weeks
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