As a board-certified clinical geneticist and medical biochemical geneticist, I care for patients of all ages with genetic and inherited metabolic disorders. In the General Genetics Clinic, I evaluate patients with developmental delay, intellectual disability, autism, epilepsy, and multiple congenital anomalies. In the Metabolic Genetics Clinic, I work with a multidisciplinary team of genetic counselors, nurses, and metabolic dietitians to provide early diagnosis and individualized treatment for patients with inborn errors of metabolism.

My clinical interests include newborn screening conditions, lysosomal storage diseases, and primary mitochondrial disorders. When families come to see me, they can expect a thorough, team-based approach centered on clear communication, compassion, and collaboration.