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Chin-To Fong, M.D., Chief |
The Division of Pediatric Genetics has three major missions:
Education
The division plays a significant role in the education mission of the Department of Pediatrics, University of Rochester School of Medicine and Dentistry, and the School of Nursing. A wide range of clinical and research electives are available, including dysmorphology, inherited metabolic disorders, cytogenetics, cardiogenetics, cancer genetics, prenatal detection of birth defects, evaluation of regional genetic counseling and regional education for prevention of birth defects, and genetic counseling. The division is involved in genetics education for medical students, graduate students, residents, fellows, and members of the community.
Research
Members of the Pediatric Genetics Division are actively engaged in research initiatives in order to better understand inherited metabolic disorders of children and adults, the delivery of genetic services, and the genetics of craniofacial abnormalities and preterm delivery.
Clinical Services
Two primary clinical services offered by Pediatric Genetics are:
The Genetic Consultations Clinic provides diagnostic genetic evaluations of children and adults who have birth defects, mental retardation, chromosome disorders, dysmorphic syndromes, craniofacial disorders, cardiogenetic syndromes, neurofibromatosis, cancer predisposition or other genetic disorders.
The Inherited Metabolic Disease Specialty Center provides newborn screening follow-up and on-going management for children with a wide range of inborn errors of metabolism. Faculty work closely with Cytogenetics, Biochemical Genetics, Prenatal Diagnosis Laboratories, Prenatal Diagnosis Program and the Pediatric Cleft and Craniofacial Center.
