Congenital Long QT Syndrome: Due to ion channel abnormalities in LQT1 and LQT2 (potassium channels) and LQT3 (sodium channels) that affect cardiac replorization. [More…]
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International Anesthesia Research Society
Congenital Long QT Syndrome: Due to ion channel abnormalities in LQT1 and LQT2 (potassium channels) and LQT3 (sodium channels) that affect cardiac replorization. [More…]