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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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| Vydáno v: | Eur Heart J Case Rep |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6177042/ https://ncbi.nlm.nih.gov/pubmed/31020160 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ehjcr/yty083 |
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