From Book News, Inc.
Some 30 different types of muscular dystrophy are now recognized. Here, 16 chapters presented by Emery (neurology, Royal Devon & Exeter Hospital, UK) review some of the most important areas of the current state of knowledge of this group of inherited disorders. The majority of the papers are devoted to individual explanations of the more prominent dystrophies. Other topics include medical management and treatment of muscular dystrophy, respiratory care, gene and cell therapy for primary myopathies, surgical management of muscular dystrophy, and animal models of muscular dystrophy.Book News, Inc., Portland, OR

Book Description
The muscular dystrophies are an important group of inherited disorders. They are characterized by muscle wasting and weakness, but vary considerably in their clinical manifestations and severity. This text reviews our understanding of the most important of these disorders. In many instances, the genes and protein products responsible for the dystrophies have been identified and it is now possible to establish a precise diagnosis, detect preclinical cases, identify carriers and offer prenatal dianostic testing. The book goes on to describe the opportunities for management of the symptoms through respiratory care, physiotherapy and surgical correction of contracture, and examines the potential, in the future, for effective treatment utilizing the new techniques of gene and cell therapy. Professor Emery has invited chapters from the leading international experts in the field providing a unique insight into the current situation and the hopes for the future.

Book Info
Royal Devon & Exeter Hospital, UK. Reviews current understanding of these disorders. Describes the opportunities for management of the symptoms through respiratory care, physiotherapy and surgical correction of contractures, and examines the potential for effective treatment utilizing the new techniques of gene and cell therapy.