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Lookup NU author(s): Emerita Professor Katherine Bushby,
Dr Fiona Norwood,
Professor Volker StraubORCiD
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
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. © 2006 Elsevier B.V. All rights reserved.
Author(s): Bushby K, Norwood F, Straub V
Publication type: Review
Publication status: Published
Journal: Biochimica et Biophysica Acta - Molecular Basis of Disease
Print publication date: 01/02/2007
ISSN (print): 0925-4439
ISSN (electronic): 0006-3002
PubMed id: 17123791