ALPORT SYNDROME

Course overview

AS, also known as hereditary nephritis, is a relatively rare inherited renal disease caused by mutations in type IV collagen chains within the basement membranes of the glomerulus, cochlea, and eyes. This continuing education module is designed to give the reader/learner an increased understanding of AS, 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.