GRISCELLI SYNDROME

Course overview

Griscelli syndrome (GS) refers to 3 rare, potentially fatal, autosomal recessive disorders, each caused by a mutation in a different gene. GS is characterized by hypopigmentation of the skin and hair. This continuing education module is designed to give the reader/learner an increased understanding of Griscelli 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.