The Division of Genetics and Genomics offers a variety of programs offering integrated care for patients with different genetic conditions. They include the following — but if you don’t see your condition represented, or are not sure which program is most appropriate, please contact us.
Specialty genetics clinics
Brain Development and Genetics Clinic: Bridging the fields of neurology, cardiology, and genetics, the BrDG Clinic helps patients with disorders of brain development or brain structure.
Cardiovascular Clinic for Brain Development: Caring for patients with periventricular nodular heterotopia (PVNH), a developmental brain disorder that also causes cardiovascular disease.
Cardiovascular Genetics Program: Staffed by cardiologists and clinical geneticists, this clinic serves children and adults with genetic heart conditions such as Marfan syndrome, Noonan syndrome, and Velo-Cardio-Facial syndrome.
Connective Tissue Genetics Program: Providing integrated care for patients of all ages with connective tissue diseases, including Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, and others.
EpiChroma Clinic: A specialty clinic for children and adults with known or suspected epigenetic or chromatin disorders, which affect genes that regulate which other genes are turned on or off.
Fragile X Program: Providing diagnostic evaluations, genetic counseling, occupational therapy, and behavioral and developmental services to children and adults with Fragile X syndrome.
Galactosemia Program: Providing comprehensive care for children and adults with galactosemia caused by GALT enzyme deficiency, and the related disorders of GALE and GALK deficiency.
Lysosomal Storage Program: Bringing together specialists in genetics, metabolism, cardiology, and neurology to serve families with Gaucher disease, Tay-Sachs disease, and related disorders.
Metabolism Program: Providing comprehensive evaluation and treatment for infants, children, and adolescents with a wide variety of metabolic disorders.
Multidisciplinary Neurofibromatosis (NF) Program: Offering comprehensive diagnostic evaluations, genetic counseling, and follow-up care by pediatric specialists from many medical areas, including ophthalmology, endocrinology, orthopedics, and neuro-oncology.
Pediatric Cancer Genetic Risk Program: Providing integrated care to patients and their families whose condition or family history suggests an increased risk of cancer.
