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Myotonic Dystrophy (The Facts)
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Table of Contents

1: What is Myotonic dystrophy? 2: Muscle symptoms and Myotonic dystrophy 3: Looking ahead 4: Not just a muscle disease 5: Children with Myotonic dystrophy 6: 'Type 2' Myotonic dystrophy 7: Family aspects and genetic risks 8: Advances in research 9: Support and information 10: Management and treatment now 11: The future-towards effective prevention and cure for Myotonic dystrophy 12: Conclusion Appendices Bibliography Index

Promotional Information

Endorsed by the Myotonic Dystrophy Foundation (US) and the Myotonic Dystrophy Support Group (UK)

About the Author

Peter Harper is a University Research Professor in Human Genetics at Cardiff University, Wales. He is a member of the UK's Advisory Committee on Genetic Testing, and has a long-standing research interest in inherited neurological disorders, especially Huntington disease and Myotonic dystrophy.

Reviews

From the previous edition `You couldn't ask for a better book about this complex disease...For anyone with this condition in the family, it's a must read at a bargain price.' Quest: the Journal of the Muscular Dystrophy Association, Vol 9, No 5 `. . . the first book to be published for lay people who have the condition. It is written clearly for people with no medical expertise.' Yours `This book is a gem that patients with this condition will want to read and own.' Doody's Journal

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