I have a strong interest in the diagnosis and management of genetic conditions. As a Clinical Associate Professor in the Department of Pediatrics at Stanford University my primary focus in the evaluation of dysmorphology syndromes, craniofacial disorders, and perinatal genetics. I am passionate about providing inclusive, just, and equitable care; dedication to my patients through collaborative research; and physician and team wellness. My overall investigative interests stem from wanting to find genetic answers for patients and their families and provide support for the rare disease community.