Extension of the clinical range of facioscapulohumeral dystrophy: report of six cases

Consensual diagnostic criteria for facioscapulohumeral dystrophy (FSHD) include onset of the disease in facial or shoulder girdle muscles, facial weakness in more than 50% of affected family members, autosomal dominant inheritance in familial cases, and evidence of myopathic disease in at least one...

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Bibliographic Details
Main Authors: van der Kooi, A J, Visser, M, Rosenberg, N, van den Berg-Vos, R, Wokke, J, Bakker, E, de Visser, M
Format: Artigo
Language:Inglês
Published: BMJ Group 2000
Subjects:
Short Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1737027/
https://ncbi.nlm.nih.gov/pubmed/10864616
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.69.1.114
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