Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk

OBJECTIVE: Myotonia Congenita (MC) is a hereditary neuromuscular disorder caused by a mutation in chloride voltage-gated channel 1 (CLCN1) gene. The incidence of MC is estimated as 1 in 100.000. The absence of left main coronary artery (LMCA) is a rare coronary anomaly. Here we present a family with...

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Detalles Bibliográficos
Autores principales: Damar, Ibrahim Halil, Eroz, Recep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Istanbul Medeniyet University 2019
Materias:
Original Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433722/
https://www.ncbi.nlm.nih.gov/pubmed/32821464
http://dx.doi.org/10.5222/MMJ.2019.93357

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433722/
https://www.ncbi.nlm.nih.gov/pubmed/32821464
http://dx.doi.org/10.5222/MMJ.2019.93357

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