Pediatric Clinical Genetics

The mission of the pediatric clinical genetics is to provide excellent, comprehensive care to patients and families with known genetic or suspected genetic disorders.

Our services include clinical evaluation and risk assessment, genetic counseling, and genetic testing. We also provide ongoing care for patients with genetic conditions, coordinate multidisciplinary care, and help patients access resources related to their condition.

Our team of highly specialized, internationally recognized physicians, genetic counselors, and nurses provide clinical services to children and adults with complex disorders including autism, epilepsy, congenital heart disease, cardiac disease, birth defects, cancer, neurofibromatosis, von Hippel Lindau, skeletal dysplasias, eye diseases, hearing loss, intellectual disability, and a wide variety of rare genetic disorders.