LEOPARD SYNDROME

Course overview

LEOPARD syndrome (LS) is typically an autosomal dominant condition caused by a genetic mutation, usually of the PTPN11 gene. This continuing education module is designed to give the reader/learner an increased understanding of LS, including its clinical presentation, symptoms, and treatment, and to aid in caring for the patient 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.