HOYERAAL-HREIDARSSON SYNDROME

Course overview

Hoyeraal-Hreidarsson syndrome (HHS) is a recessive disorder caused by a mutation in the DKC1 gene, or TERT genes; some experts believe that HHS is a severe variant of dyskeratosis congenita (DKC; i.e., a rare syndrome characterized by progressive bone marrow failure). This continuing education module is designed to give the reader/learner an increased understanding of HHS, including its clinical presentation, symptoms, and treatment, and to aid in caring 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.