9780198525868-0198525869-Myotonic Dystrophy: The Facts (Oxford Medical Publications)

Myotonic Dystrophy: The Facts (Oxford Medical Publications)

ISBN-13: 9780198525868
ISBN-10: 0198525869
Edition: 1
Author: Peter Harper
Publication date: 2002
Publisher: Oxford University Press
Format: Paperback 128 pages
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Book details

ISBN-13: 9780198525868
ISBN-10: 0198525869
Edition: 1
Author: Peter Harper
Publication date: 2002
Publisher: Oxford University Press
Format: Paperback 128 pages

Summary

Myotonic Dystrophy: The Facts (Oxford Medical Publications) (ISBN-13: 9780198525868 and ISBN-10: 0198525869), written by authors Peter Harper, was published by Oxford University Press in 2002. With an overall rating of 4.0 stars, it's a notable title among other Genetic (Diseases & Physical Ailments, Musculoskeletal Diseases, Health Care Delivery, Administration & Medicine Economics) books. You can easily purchase or rent Myotonic Dystrophy: The Facts (Oxford Medical Publications) (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 $0.3.

Description

Myotonic dystrophy is part of the group of muscular dystrophies. It is the commonest inherited muscular dystrophy and has a profound effect on indviduals who are diagnosed with the disease and their families. It is present for many depths of a patient's life and has many attendant implications. Associated problems with other organs of the body, for example, which does not occur in the other dystrophies, making this very distinctive disorder, and very troubling one for those close to it. This book covers a wide range of aspects of the disease, and explains in simple terms exactly what the condition is, what the symptoms are and how they can or might develop. Also discussed is how to present them, or spot them early enough to treat them, and so limit any potential debilitation. Routes for further study are gone into, as it is not claimed that the book is exhaustive, it does not, for example, cover the very rarest manifestations of the illness. Self education is encouraged and this book gives anyone interested the tools with which to find out more and empower themselves by taking an active role in their own treatment. Most importantly, it carries the message that there is hope, something can be done, even if there is, as yet, no actual cure. Any patient who has left a diagnostic consultation with the impression that there is nothing to be done will find this a great source of hope and strength.
There are few clinicians more experienced in this field than Peter Harper who has studied and written extensively on the subject.

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