Cardiac Involvement and Arrhythmias Associated with Myotonic Dystrophy

Myotonic dystrophy is an autosomal dominant genetic disease of nucleotide expansion resulting in neuromuscular disease with two distinct subtypes. There are significant systemic manifestations of this condition including progressive muscular decline, neurologic abnormalities, and cardiac disease. Gi...

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Bibliographic Details
Main Authors: Daniel McBride, Amrish Deshmukh, Supriya Shore, Melissa A. Elafros, Jackson J. Liang
Format: Article
Language:English
Published: IMR Press 2022-04-01
Series:Reviews in Cardiovascular Medicine
Subjects:
Online Access:https://www.imrpress.com/journal/RCM/23/4/10.31083/j.rcm2304126