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Dr. Enns is a Professor of Pediatrics and Director of the Biochemical Genetics Program at Stanford University. After receiving his medical degree from the University of Glasgow, he trained in Pediatrics at Children's Hospital Los Angeles, and in Clinical Genetics and Clinical Biochemical Genetics at the University of California, San Francisco.

He has extensive experience in the diagnosis and management of inborn errors of metabolism, including congenital disorders of glycosylation, mitochondrial disorders, and lysosomal storage disorders. Dr. Enns also performs translational research focusing on the development of a sensitive panel of redox biomarkers to study disorders of energy metabolism, and participates in clinical trials aimed at developing novel treatments for inborn errors of metabolism.