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A303 GASTROINTESTINAL MANIFESTATIONS IN PATIENTS WITH CONGENITAL MYOTONIC DYSTROPHY
BACKGROUND: Myotonic Dystrophy type 1 is an autosomal dominant, multisystem disease characterized by muscle weakness and myotonia. Phenotypes include congenital, childhood and classic adult onset. Congenital Myotonic Dystrophy (CDM) is the most severe occurring in neonates, characterized by severe h...
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| Publicado no: | J Can Assoc Gastroenterol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6508232/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwy009.303 |
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