Teaching NeuroImages: Coats disease revealing facioscapulohumeral muscular dystrophy

Teaching NeuroImages: Coats disease revealing facioscapulohumeral muscular dystrophy

Author Sgobbi de Souza, Paulo Victor Autor UNIFESP Google Scholar
Vieira de Rezende Pinto, Wladimir Bocca Autor UNIFESP Google Scholar
de Rezende Batistella, Gabriel Novaes Autor UNIFESP Google Scholar
Dias, Renan Braido Autor UNIFESP Google Scholar
Bulle Oliveira, Acary Souza Autor UNIFESP Google Scholar
Abstract A 21-year-old Brazilian woman presented with mild facial muscle weakness, scapular winging and an asymmetric shoulder girdle, and peroneal weakness. Medical history disclosed mildly symptomatic Coats disease (CD) (figure). Muscle MRI studies were highly suggestive of facioscapulohumeral muscular dystrophy type 1 (FSHD1) (figure) and genetic testing confirmed this diagnosis.
xmlui.dri2xhtml.METS-1.0.item-coverage Philadelphia
Language English
Date 2016
Published in Neurology. Philadelphia, v. 87, n. 4, p. E39-E39, 2016.
ISSN 0028-3878 (Sherpa/Romeo, impact factor)
Publisher Lippincott Williams & Wilkins
Extent E39-E39
Origin http://dx.doi.org/10.1212/WNL.0000000000002899
Access rights Open access Open Access
Type Editorial
Web of Science ID WOS:000381472000004
URI https://repositorio.unifesp.br/handle/11600/57528

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