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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...
Autores principales: | Bielen, Jurgen, Schepers, Steven, Termote, Bruno, Vanwyck, Rik, Souverijns, Geert |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ubiquity Press
2016
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Materias: | |
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 |
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