Revised Genetic Classification of Limb Girdle Muscular Dystrophies

被引:7
|
作者
Magri, F. [1 ]
Brajkovic, S. [1 ]
Govoni, A. [1 ]
Brusa, R. [1 ]
Comi, G. P. [1 ]
机构
[1] Univ Milan, IRCCS, Fdn Ca Granda Osped Maggiore Policlin,Dino Ferrar, Dept Pathophysiol & Transplantat DEPT,Neurosci Se, I-20122 Milan, Italy
关键词
Classification; DNAJB6; genetics; isoprenoid synthase domain-containing (ISPD) gene; limb girdle muscular dystrophy; LGMD2R; transportin; 3; WALKER-WARBURG-SYNDROME; DEFECTIVE GLYCOSYLATION; GLYCOPROTEIN COMPLEX; ALPHA-DYSTROGLYCAN; ISPD GENE; MUTATIONS; SARCOGLYCAN; LOCUS; FORM; IDENTIFICATION;
D O I
10.2174/1566524014666141010130244
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Limb girdle muscular dystrophies (LGMD) are a heterogeneous group of inherited progressive muscle disorders affecting predominantly the shoulder and pelvic girdle muscles. They present both with autosomal dominant and autosomal recessive patterns of inheritance. Recent development, including results from Next Generation Sequencing technology, expanded the number of recognised forms. Therefore a revised genetic classification that takes into account the novel entities is needed, allowing clinicians and researchers to refer to a common nomenclature for diagnostic and research purposes.
引用
收藏
页码:934 / 943
页数:10
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