What's in a name? The clinical features of facioscapulohumeral muscular dystrophy
Publication year
2016Source
Practical Neurology, 16, 3, (2016), pp. 201-7ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Journal title
Practical Neurology
Volume
vol. 16
Issue
iss. 3
Page start
p. 201
Page end
p. 7
Subject
Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical NeuroscienceAbstract
Facioscapulohumeral muscular dystrophy (FSHD) is an inherited and progressive muscle disorder. Although its name suggests otherwise, it comprises weakness of the facial, shoulder and upper arm muscles, and also of the trunk and leg muscles. Its severity and disease course vary greatly and mild or early FSHD can be difficult to recognise. Knowledge of its subtle signs and symptoms can lead directly to the correct diagnosis without diagnostic delay and without needing multiple diagnostic procedures. We give an overview of the signs and symptoms of FSHD in severe as well as in mild cases, to facilitate correct and instant recognition of this relatively common muscle disorder.
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- Academic publications [234316]
- Faculty of Medical Sciences [89180]
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