Andersen-Tawil syndrome is a rare type of channelopathy characterized by the presence of periodic paralysis, cardiac arrhythmia (prolonged QT interval or ventricular arrhythmia) and distinct dysmorphic abnormalities. It is a type of potassium channelopathy that occurs sporadically or by autosomal dominant inheritance. We report a 14 year old boy with Andersen-Tawil syndrome.
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea
Joh, Dong Hoo
Park, Jin Su
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea
Park, Jin Su
Lee, Seung-Jun
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea
Lee, Seung-Jun
Lee, Hancheol
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea
Lee, Hancheol
Kim, Wonjin
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea
Kim, Wonjin
Joung, Boyoung
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Yonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South KoreaYonsei Univ, Coll Med, Dept Internal Med, Div Cardiol, Seoul 120752, South Korea