In the Children’s Health Genetics clinic, we see children up to age 19 who have a known or suspected genetic condition. From chromosomal anomalies to metabolic diseases to down syndrome our providers have extensive clinical experience in diagnosing even the most complex disorders. Learn more.
ServicesEvaluation and testing for children with known or suspected inborn errors of metabolism, Prenatal screening, newborn screening and carrier screening, Interpretation of genetic test results, Family history analysis and genetic counseling to discuss reproductive options as pertains to inborn, Education about specific inborn errors of metabolism, Comprehensive case management with referral to medical specialists, community resources and support, Consultation regarding abnormal newborn screening and metabolic testing resultsAdditional ServicesHospital