
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.
This book investigates the biological mechanisms, clinical manifestations, and management strategies associated with the various forms of muscular dystrophy. Professor Alan E. H. Emery, a specialist in the field, synthesizes decades of clinical experience to provide a comprehensive resource for patients and their families. The text aims to demystify the genetic basis of these conditions while offering practical guidance on navigating the physical, educational, and emotional challenges of a diagnosis.
What You Will Find
Scope Limits
Readers frequently note the accessibility of the prose, which avoids excessive technical jargon to remain helpful for non-specialists. Experts recognize this work as a compassionate and reliable foundational resource for families seeking to understand the implications of a muscular dystrophy diagnosis.
Page Count:
160
Publication Date:
2008-01-01
Publisher:
OUP Oxford
ISBN-10:
0191580104
ISBN-13:
9780191580109
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