Overview
This book provides a full and practical account of management of myotonic dystrophy, the commonest muscular dystrophy of adult life and a condition of exceptional variability. Written for neurologists, clinical geneticists and other clinical specialities involved with the disorder, it deals with both the neurological aspects and also the wide range of systemic complications that may occur. In addition it provides details of information and support available to patients and families and gives a summary of the present state of clinical trials of therapeutic agents. These sections are preceded by general introductory chapters describing both the clinical features and also the current state of research into understanding the underlying mechanisms.
Full Product Details
Author: Peter Harper (, Professor and Consultant in Medical Genetics, Institute of Medical Genetics, University of Wales College of Medicine, Cardiff) ,
Baziel van Engelen (, Department of Neurology, University of Nijmegen, The Netherlands) ,
Bruno Eymard (, Department of Neurology, La Salpetriere Hospital, Paris, France) ,
Douglas Wilcox (, Scottish Muscle Centre, University of Glasgow, Glasgow, Scotland)
Publisher: Oxford University Press
Imprint: Oxford University Press
Dimensions:
Width: 16.10cm
, Height: 1.90cm
, Length: 24.10cm
Weight: 0.536kg
ISBN: 9780198527824
ISBN 10: 0198527829
Pages: 264
Publication Date: 15 January 2004
Audience:
Professional and scholarly
,
Professional & Vocational
Format: Hardback
Publisher's Status: Active
Availability: To order
Stock availability from the supplier is unknown. We will order it for you and ship this item to you once it is received by us.
Reviews
This book written by the main world experts in the field is a practical outline for both the clinicians and families. I strongly recommend it. European Journal of Paediatric Neurology, Vol 10 ... illustrates all the various clinical aspects of this complex disease and gives insight into the pathogenesis and possibilities of the management of each complication at the different stages of myotonic dystrophy. The completeness of the data presented in each chapter is imporessive. The chapters are well structured and the illustrations are clear and informative. The flow charts are adequately structured and easy to understand. The references are well-selected and up-to-date. All chapters are written by renowned experts in the field of the myotonic dystrophies and neuromuscular diseases. It is a most educative book for clinicians working in the field of the neuromuscular diseases and for geneticists responsible for the genetic counselling of patients with myotonic dystrophy. Human Genetics ... a book that offers a wealth of up-to-date, practical and relevant information. Reflecting the central role of neuromuscular assessment and clinical management issues, this book is to be recommended as an essential reference for every neurologist involved in the care of patients with myotonic dystrophy. Neuromuscular Disorders, 14
