CHARGE SYNDROME

Course overview

CHARGE syndrome (CS) is a genetic disorder that is either inherited in an autosomal dominant pattern or is caused by a spontaneous mutation in the CHD7 gene. The term CHARGE is based on the characteristics of CS, which are coloboma, heart anomalies, choanal atresia, retardation of growth and development, genital anomalies, and ear anomalies. This continuing education module is designed to give the reader/learner an increased understanding of CHARGE 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.