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ColumbiaDoctors world-renowned geneticists are committed to the proper diagnosis and treatment of children and families with complex genetic problems and birth defects. We lead a variety of cutting edge programs that enable patients to receive the best clinical care. Some of the special programs offered by clinical genetics are:
Columbia's pediatrics team offers advanced genetic testing for children and families with autism spectrum disorders in New York City.
The Cardiogenetics Program provides genetic evaluation and continued care for individuals and families with known or suspected cardiac conditions.
The Pediatric Craniofacial Program in New York City, provides diagnosis, genetic testing and counseling, and treatment of a wide variety of craniofacial abnormalities.
Columbia's pediatric specialists provide genetic counseling for families of cystic fibrosis patients in New York City, Westchester, and the surrounding region.
The DISCOVER Program integrates excellent clinical care with cutting-edge research to rapidly arrive at a diagnosis of rare diseases and complex conditions.
The Inherited Metabolic Disease Program provides expert diagnosis, management, and genetic counseling for children with inherited metabolic disorders and their families.
The Neurofibromatosis Program, located in NewYork-Presbyterian Morgan Stanley Children's Hospital, provides comprehensive care for people with NF1, NF2, and Schwannomatosis.
Columbia's Vascular Anomalies Program provides expert care for children and adults with vascular anomalies—problems that develop in the blood and lymphatic vessels, causing birthmarks or growths.