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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Publicat a:J Can Assoc Gastroenterol
Autors principals: Bortolin, K, Ceballos Saenz, D, Zizzo, A, Campbell, C
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2018
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Accés en línia: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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