Ventricular Tachyarrhythmias in a Patient with Andersen-Tawil Syndrome

Andersen-Tawil syndrome (ATS), a rare autosomal dominant disorder, is characterized by periodic paralysis, dysmorphic features and cardiac arrhythmias. This syndrome is caused by mutations of KCNJ2 gene, which encodes inward rectifying potassium channel. Here, we report an 18-year-old girl who was p...

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Detalles Bibliográficos
Autores principales: Pyo, Jung Yoon, Joh, Dong Hoo, Park, Jin Su, Lee, Seung-Jun, Lee, Hancheol, Kim, Wonjin, Joung, Boyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Cardiology 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569570/
https://www.ncbi.nlm.nih.gov/pubmed/23407770
http://dx.doi.org/10.4070/kcj.2013.43.1.62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569570/
https://www.ncbi.nlm.nih.gov/pubmed/23407770
http://dx.doi.org/10.4070/kcj.2013.43.1.62

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