ANDERSEN-TAWIL SYNDROME

Course overview

Andersen-Tawil syndrome (ATS) is a rare ion channel caused by a genetic mutation in the KCNJ2 gene. The mutation that causes ATS is believed to alter potassium channels in such a way that the flow of potassium ions is disrupted in the brain, heart, and skeletal muscles. This continuing education module is designed to give the reader/learner an increased understanding of Andersen-Tawil syndrome, its clinical presentation, symptoms, and treatment for patients with this diagnosis. Readers may explore any or all of the topics. One contact hour of continuing education credit is available for those who successfully complete the post-test and evaluation form.