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...

Full description

Saved in:
Bibliographic Details
Main Authors: Lallemand, Bénédicte, Clementy, Nicolas, Bernard-Brunet, Anne, Pierre, Bertrand, Corcia, Philippe, Fauchier, Laurent, Raynaud, Martine, Pellieux, Sybille, Babuty, Dominique
Format: Artigo
Language:Inglês
Published: BMJ Group 2011
Subjects:
Heart Rhythm Disorders
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3262987/
https://ncbi.nlm.nih.gov/pubmed/22038543
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/heartjnl-2011-300143
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items