HYPERAMMONEMIA-HYPERORNITHINEMIA-HOMOCITRULLINEMIA SYNDROME

Course overview

Hyperammonemia-hyperornithinemia-homocitrullinemia (HHH; also known as mitochondrial ornithine transporter deficiency) syndrome is an inborn error of metabolism of the urea cycle and ornithine degradation pathway. This continuing education module is designed to give the reader/learner an increased understanding of HHH syndrome, 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.