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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Istanbul Medeniyet University
2019
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| Materias: | |
| 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 |