
Muscular Dystrophy
Alan E.H. Emery(Author)
Oxford University Press
3rd Edition
Published on 6. March 2008
Book
Paperback/Softback
160 pages
978-0-19-954216-1 (ISBN)
Description
The muscular dystrophies are a group of genetic diseases that severely affect children and adults. For sufferers and their family, the illness presents enormous physical and psychological challenges. Written specifically for people with muscular dystrophy and their families, this book answers many of the questions asked about how and why muscular dystrophy occurs, and how it will affect the life of a recently diagnosed child.
As well as presenting the reader with advice and an explanation of muscular dystrophy, the book also guides the reader towards further information on societies and support groups around the world, and reliable internet resources. It also contains a full glossary to aid the reader in their understanding of the disease.
The different types of muscular dystrophy are described throughout with a minimum of technical jargon. Questions relating to exercise, physiotherapy, surgery, and the emotional effects of the diseases are answered, and advice is given on the problems of schooling and choice of career.
Since publication of the first edition in 1994, the genes for almost all the different types of dystrophy have been identified, enabling prevention through genetic counselling, therefore relieving some of the worry for affected families. Drawn from his many years of experience treating patients, Professor Emery provides authoritative, yet compassionate advice for people living with this illness.
As well as presenting the reader with advice and an explanation of muscular dystrophy, the book also guides the reader towards further information on societies and support groups around the world, and reliable internet resources. It also contains a full glossary to aid the reader in their understanding of the disease.
The different types of muscular dystrophy are described throughout with a minimum of technical jargon. Questions relating to exercise, physiotherapy, surgery, and the emotional effects of the diseases are answered, and advice is given on the problems of schooling and choice of career.
Since publication of the first edition in 1994, the genes for almost all the different types of dystrophy have been identified, enabling prevention through genetic counselling, therefore relieving some of the worry for affected families. Drawn from his many years of experience treating patients, Professor Emery provides authoritative, yet compassionate advice for people living with this illness.
Reviews / Votes
This is a unique book written with expert finesse. It should be in all neuromuscular clinics and available for patients to read. * Doody's Notes * Review from previous edition For the 2nd Edition: "No family (with a member who has any form of muscular dystrophy (MD)) should be without a copy of Alan Emery's book, nor should any PCT or medical training unit fail to have easy access to the copy... Apart from the easy 'accessibility' of [the book], the chapter layout makes it eminently usable as a reference, a really useful handbook for anyone with an interest in MD". * Stephen Gazzard, Muscular Dystrophy Campaign, Oxford (Published in 'Neuromuscular Disorders', 14 (2004) 83-84 *More details
Series
Edition
3rd Revised edition
Language
English
Place of publication
Oxford
United Kingdom
Edition type
Revised edition
Illustrations
12 Black and white photos and 13 line drawings
Dimensions
Height: 200 mm
Width: 130 mm
Thickness: 10 mm
Weight
171 gr
ISBN-13
978-0-19-954216-1 (9780199542161)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

Alan E.H. Emery
Muscular Dystrophy
E-Book
03/2008
1st Edition
Oxford University Press
€30.27
Available for download
Previous edition

Alan E. H. Emery
Muscular Dystrophy
Book
05/2000
2nd Edition
Oxford University Press
€23.52
Article exhausted; check for reprint
Person
Professor Alan E. H. Emery is Emeritus Professor of Human Genetics at the University of Edinburgh and Chief Scientific Advisor for the European Neuromuscular Centre. He continues his research through the University of Oxford.
Content
1. What is muscular dystrophy? ; 2. Confirming the diagnosis ; 3. Different types of muscular dystrophy ; 4. Treatment ; 5. Living with muscular dystrophy ; 6. Education and employment ; 7. Inheritance and genetic counselling ; 8. Professional and voluntary support ; 9. The future ; 10. Further reading and useful contacts