|Schedule An Appointment||Clinical Office Address|
|(801) 213-3599||Primary Children's Hospital
100 N Mario Capecchi Drive
Salt Lake City, UT 84113
Dr. Stevenson received his medical degree from the University of Utah School of Medicine, completed his Pediatric residency at the University of New Mexico, and his Medical Genetics Fellowship at the University of Utah. He has been on faculty at the University of Utah within the Department of Pediatrics since 2005 and is currently an Assistant Professor of Pediatrics. Dr. Stevenson is board-certified in Pediatrics and Medical Genetics.
Dr. Stevenson sees a variety patients in the University of Utah general medical genetics clinic at Primary Children’s Medical Center. His specific clinical interests include disorders of the Ras/MAPK pathway (e.g. neurofibromatosis type 1, Noonan syndrome, Costello syndrome, CFC syndrome), vascular anomalies, and bone disorders. He is an attending physician at the Osteogenesis Imperfecta Clinic at the Salt Lake City Shriners Hospital and the Hereditary Hemorrhagic Telangiectasia (HHT) Clinic at the University of Utah.
Dr. Stevenson’s research interests focus on understanding the pathophysiology of the musculoskeletal abnormalities of the Rasopathies, with a primary focus on scoliosis and tibial dysplasia in neurofibromatosis type 1. He also conducts research on Prader-Willi syndrome, vascular malformations, and the genetics of non-syndromic orthopedic manifestations such as developmental dysplasia of the hip.
Board Certification and Academic Information
|Academic Departments||Pediatrics - Associate Professor
|Academic Divisions||Pediatric Genetics
|Board Certification||American Board of Medical Genetics (Sub: Clinical Genetics)