The evolution of infrahissian conduction time in myotonic dystrophy patients: clinical implications

BACKGROUND: Myotonic dystrophy (MD1) is a hereditary autosomal dominant disease with variable penetrance. Cardiac conduction disturbances are frequent and may be responsible for sudden death, but its progression was heretofore unknown. AIMS: The aim of the study was to analyse the natural history of...

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Detalles Bibliográficos
Autores principales: Lallemand, Bénédicte, Clementy, Nicolas, Bernard-Brunet, Anne, Pierre, Bertrand, Corcia, Philippe, Fauchier, Laurent, Raynaud, Martine, Pellieux, Sybille, Babuty, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2011
Materias:
Heart Rhythm Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262987/
https://www.ncbi.nlm.nih.gov/pubmed/22038543
http://dx.doi.org/10.1136/heartjnl-2011-300143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262987/
https://www.ncbi.nlm.nih.gov/pubmed/22038543
http://dx.doi.org/10.1136/heartjnl-2011-300143

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