Ventricular tachyarrhythmias in a patient with Andersen-Tawil syndrome

Andersen-Tawill 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...

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Veröffentlicht in:Korean circulation journal 2013, 43(1), , pp.62-65
Hauptverfasser: Pyo, Jung Yoon, Joh, Dong Hoo, Park, Jin Su, Lee, Seung-Jun, Lee, Hancheol, Kim, Wonjin, Joung, Boyoung
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Sprache:eng
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Zusammenfassung:Andersen-Tawill 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 presented with life-threatening cardiac arrhythmia and acute respiratory distress. She was diagnosed with ATS, based on dysmorphic features, ventricular arrhythmia, and periodic paralysis. This is the first case to be reported in Korea who experienced a fatal cardiac arrest and respiratory failure caused by ATS.
ISSN:1738-5520
1738-5555
DOI:10.4070/kcj.2013.43.1.62