Held four times per year, the St. Luke's Children's Metabolic Clinic provides diagnostic and management services for children with confirmed or suspected metabolic inborn errors. Our team of experts specializes in metabolic genetics, biochemical genetics, inborn errors of metabolism, PKU, mitochondrial disorders, galactosemia, biotinidase deficiency, and enzyme replacement therapy.
Services range from diagnosis and evaluation to management, genetic counseling, and treatment.
We welcome referrals at any age. Patients are generally referred through their primary care physicians or other specialist. However, appropriate self-referrals are accepted.