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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Detalles Bibliográficos
Autores principales: McBride, Daniel, Deshmukh, Amrish, Shore, Supriya, Elafros, Melissa A., Liang, Jackson J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9518819/
https://www.ncbi.nlm.nih.gov/pubmed/36177340
http://dx.doi.org/10.31083/j.rcm2304126

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9518819/
https://www.ncbi.nlm.nih.gov/pubmed/36177340
http://dx.doi.org/10.31083/j.rcm2304126

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