COFFIN-LOWRY SYNDROME

Course overview

Coffin-Lowry syndrome (CLS) is an X-linked genetic disorder with variable expression that is characterized by craniofacial and skeletal abnormalities, mental retardation, and hypotonia. This continuing education module is designed to give the reader/learner an increased understanding of Coffin-Lowry 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.