Facioscapulohumeral Dystrophy-Reference-Cited by-同舟云学术

Facioscapulohumeral Dystrophy

Published:2008-01-01 Issue:1 Volume:88 Page:105-113
ISSN:0031-9023
Container-title:Physical Therapy
language:en
Short-container-title:

Author:

Pandya Shree¹,King Wendy M²,Tawil Rabi³

Affiliation:

1. S Pandya, PT, MS, is Assistant Professor of Neurology and Physical Medicine and Rehabilitation, School of Medicine and Dentistry, University of Rochester, Rochester, NY 14627 (USA)

2. WM King, PT, BA, is Clinical Assistant Professor of Neurology, Department of Neurology, Ohio State University, Columbus, Ohio

3. R Tawil, MD, is Professor of Neurology, Department of Neurology, University of Rochester

Abstract

Facioscapulohumeral dystrophy (FSHD) is the third most common inherited muscular dystrophy after Duchenne dystrophy and myotonic dystrophy. Over the last decade, major advances have occurred in the understanding of the genetics of this disorder. Despite these advances, the exact mechanisms that lead to atrophy and weakness secondary to the genetic defect are still not understood. The purposes of this article are to increase awareness of FSHD among clinicians; to provide an update regarding the genetics, clinical features, natural history, and current management of FSHD; and to discuss opportunities for research.

Publisher

Oxford University Press (OUP)

Subject

Physical Therapy, Sports Therapy and Rehabilitation

Link

http://academic.oup.com/ptj/article-pdf/88/1/105/31666506/ptj0105.pdf

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