Myotonic Dystrophy

Myotonic dystrophy 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.

First edition and reception

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.

New edition features

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 ongoing worldwide 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.