Imaging in Myotonic Dystrophy Type 1 – Case Reports

Myotonic dystrophy type 1 (DM1) is the most common of the muscular dystrophies. It is an autosomal dominant neuromuscular disorder with multisystem involvement, including the central nervous system. Two DNA-proven cases are presented. Patients reported are siblings showing features of DM1 on magneti...

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Detalles Bibliográficos
Autores principales: Bielen, Jurgen, Schepers, Steven, Termote, Bruno, Vanwyck, Rik, Souverijns, Geert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ubiquity Press 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100612/
https://www.ncbi.nlm.nih.gov/pubmed/30151479
http://dx.doi.org/10.5334/jbr-btr.994

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100612/
https://www.ncbi.nlm.nih.gov/pubmed/30151479
http://dx.doi.org/10.5334/jbr-btr.994

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