Provide outpatient and inpatient clinical genetics consultation, with an emphasis on but not limited to inborn errors of metabolism (e.g., lysosomal storage disorders, galactosemia, urea cycle disorders, and related conditions) across the pediatric-to-adult lifespan. This faculty member will help lead metabolic patient care alongside our existing metabolic genetics team, manage a mixed pediatric and adult caseload, and contribute to resident education, newborn screening follow-up, and clinical research.