Asymptomatic ventricular tachycardia: diagnostic pitfalls of Andersen–Tawil syndrome—a case report

BACKGROUND: Andersen–Tawil syndrome (ATS) is a rare arrhythmia disorder caused by a mutation in the KCNJ2 gene. Typical presentation includes a triad of cardiac arrhythmia, dysmorphia, and periodic paralysis. However, KCNJ2 mutations can mimic other disorders such as catecholaminergic polymorphic ve...

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Detalles Bibliográficos
Autores principales: Nguyen, Dustin, Ferns, Sunita J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177042/
https://www.ncbi.nlm.nih.gov/pubmed/31020160
http://dx.doi.org/10.1093/ehjcr/yty083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177042/
https://www.ncbi.nlm.nih.gov/pubmed/31020160
http://dx.doi.org/10.1093/ehjcr/yty083

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