The limb-girdle muscular dystrophies - Diagnostic strategies

被引:20
作者
Bushby, Kate
Norwood, Fiona
Straub, Volker
机构
[1] Int Ctr Life, Inst Human Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[2] Kings Coll Hosp London, King Reg Neurosci Ctr, London SE5 9RS, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2007年 / 1772卷 / 02期
关键词
limb girdle muscular dystrophies; muscular dystrophy differential diagnosis; muscular dystrophy management;
D O I
10.1016/j.bbadis.2006.09.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The limb-girdle muscular dystrophies are a group of disorders where our understanding of their underlying molecular basis has made huge strides over the past years, revealing great heterogeneity at the clinical and molecular level. The availability of direct protein and/or gene based approaches to diagnosis means that these disorders can now be precisely defined, and such definition of a precise diagnosis is increasingly allowing directed management for these diseases by the ability to predict specific complications such as those of the cardiac or respiratory systems. An algorithm combining clinical, biochemical and molecular testing is described which will aid precision of diagnosis and direct specific testing towards the cases most likely to benefit. This brings advantages for the patients of today in recognising the specific risks of their disorders, and in the future will be the starting point for specific gene and protein based therapies. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:238 / 242
页数:5
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