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Home > Care & Treatment > Genetic Disorders > Meet Our Team
Chief, Division of Pediatric Genetics and Metabolism Associate Professor of Pediatrics
Hearing loss; birth defects; and inborn errors of metabolism.
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Associate Professor of Pediatrics
Metabolic disorders; medical genetics; dysmorphology; epidemiology; and mitochondrial disorders.
Professor of Pediatrics
Inborn errors of metabolism including mucopolysaccharidoses, lysosomal and glycogen storage disorders; disorders of amino acid and carbohydrate metabolism; organic acidurias; and urea cycle disorders.
Professor of Pediatrics and Genetics
Genetics of hearing loss; genetic and chromosomal syndromes; ethical issues in genetics; and newborn screening.
N-of-1 treatment clinical trials for rare inborn errors of metabolism; diagnosis and management of inborn errors of metabolism.
You’ll need a physician’s referral for genetic testing and counseling. For more information, talk to your doctor or call us at 984-974-1401.
N.C. Children's Hospital
101 Manning Drive
Chapel Hill, NC 27514
UNC Department of Pediatrics
Medical Foundation of North Carolina
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