The Metabolic Clinic provides lifelong follow-up and treatment for individuals diagnosed with inborn errors of metabolism through newborn screening.
The NBS Endocrine Follow-Up Program is located at the University of Michigan C.S. Mott Children’s Hospital Division of Endocrinology which coordinates follow-up for babies who test positive for congenital hypothyroidism and congenital adrenal hyperplasia (CAH).
This public health program, required by Michigan Law, helps find babies with rare but serious medical conditions that require early treatment.
This overview of Michigan’s EHDI Program explains the process of identification, intervention, and follow-up for newborns with congenital hearing loss.