Myotonic Dystrophy / Edition 2

Myotonic Dystrophy / Edition 2

by Peter Harper
ISBN-10:
019957197X
ISBN-13:
9780199571970
Pub. Date:
10/26/2009
Publisher:
Oxford University Press
ISBN-10:
019957197X
ISBN-13:
9780199571970
Pub. Date:
10/26/2009
Publisher:
Oxford University Press
Myotonic Dystrophy / Edition 2

Myotonic Dystrophy / Edition 2

by Peter Harper
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Overview

Myotonic dystrophy is part of the group of muscular dystrophies. It is the commonest inherited muscular dystrophy and has a profound effect on individuals who are diagnosed with the disease and their families. It is present for many decades of a patient's life but, unlike the other dystrophies, it also affects the organs in the body, making this a very distinctive disorder, and a very troubling one for those close to it.

When the first edition of Myotonic Dystropy: The Facts published in 2002, it was widely appreciated by families, support groups, professionals, and reviewers for its simple and clear approach to key practical questions. This new edition retains the same successful structure, but now includes new material on the recognition of the distinct "type 2 myotonic dystrophy," which had only just been identified at the time of the first edition. Further explanation of the advances in basic understanding of myotonic dystrophy, and additional coverage of the new approaches to therapy and management of the condition are also included, as well as comprehensive discussion of the recent on-going worlwide research.

New to this edition are "Key Facts" at the beginning of each chapter, "Frequently Asked Questions" boxes, and up-to-date contact details for worldwide myotonic dystrophy support groups.

Product Details

ISBN-13: 9780199571970
Publisher: Oxford University Press
Publication date: 10/26/2009
Series: The ^AFacts Series
Edition description: 2nd ed.
Pages: 128
Product dimensions: 5.00(w) x 7.60(h) x 0.30(d)

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.

Table of Contents

1. What is Myotonic dystrophy? 2. Muscle symptoms and Myotonic dystrophy3. Looking ahead4. Not just a muscle disease5. Children with Myotonic dystrophy6. 'Type 2' Myotonic dystrophy7. Family aspects and genetic risks8. Advances in research9. Support and information10. Management and treatment now11. The future-towards effective prevention and cure for Myotonic dystrophy12. ConclusionAppendicesBibliographyIndex
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