9780199571970-019957197X-Myotonic Dystrophy (The ^AFacts Series)

Myotonic Dystrophy (The ^AFacts Series)

ISBN-13: 9780199571970
ISBN-10: 019957197X
Edition: 2
Author: Peter Harper
Publication date: 2009
Publisher: Oxford University Press
Format: Paperback 106 pages
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Book details

ISBN-13: 9780199571970
ISBN-10: 019957197X
Edition: 2
Author: Peter Harper
Publication date: 2009
Publisher: Oxford University Press
Format: Paperback 106 pages

Summary

Myotonic Dystrophy (The ^AFacts Series) (ISBN-13: 9780199571970 and ISBN-10: 019957197X), written by authors Peter Harper, was published by Oxford University Press in 2009. With an overall rating of 4.1 stars, it's a notable title among other Genetic (Diseases & Physical Ailments, Musculoskeletal Diseases) books. You can easily purchase or rent Myotonic Dystrophy (The ^AFacts Series) (Paperback) from BooksRun, along with many other new and used Genetic books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $1.29.

Description

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.

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