Dr. Gregory Enns

Biography

Gregory Enns is a Professor of Pediatrics specializing in Medical Genetics at Stanford University. He has extensive experience in biochemical genetics and mitochondrial diseases and has been involved in numerous clinical trials aimed at developing novel treatment methodologies. His clinical focus includes the diagnosis and treatment of a variety of genetic disorders, emphasizing the use of antioxidant therapy and newborn screening techniques. Dr. Enns is board certified in Clinical Genetics and Clinical Biochemical Genetics by the American Board of Medical Genetics and Genomics. He completed his pediatric residency at Children's Hospital Los Angeles and has undergone fellowship training at UCSF Medical Center. His research interests concentrate on the diagnosis and treatment of mitochondrial disorders and lysosomal disorders, often utilizing advanced biochemical analyses and collaboration through international registries. Enns has played a key role in the North American Mitochondrial Disease Consortium and has been pivotal in studying the long-term effectiveness and safety of enzyme replacement therapies. He is actively involved in teaching and mentoring students and has contributed significantly to the field through his participation in various clinical trials.

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