Orthopaedic Disorders in Myotonic Dystrophy Type 1: descriptive clinical study of 21 patients

BACKGROUND: Myotonic Dystrophy Type 1 (DM1) is the most common form of hereditary myopathy presenting in adults. This autosomal-dominant systemic disorder is caused by a CTG repeat, demonstrating various symptoms. A mild, classic and congenital form can be distinguished. Often the quality of life is...

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Detalles Bibliográficos
Autores principales: Schilling, Lisa, Forst, Raimund, Forst, Jürgen, Fujak, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219587/
https://www.ncbi.nlm.nih.gov/pubmed/24289806
http://dx.doi.org/10.1186/1471-2474-14-338

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219587/
https://www.ncbi.nlm.nih.gov/pubmed/24289806
http://dx.doi.org/10.1186/1471-2474-14-338

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