KCNJ2 mutations lead to a cardiodysrhythmic type of periodic paralysis known as Andersen-Tawil syndrome (ATS; MIM 170390) [39], which is characterized by ventricular arrhythmias, periodic paralysis, facial and skeletal dysmorphism including hypertelorism, small mandible, cleft palate, syndactyly, clinodactyly, and scoliosis [38], [39]. The gene discussed is KCNJ2; the disease is Andersen-Tawil syndrome.