Congenital Disorders Genetic Testing

Congenital disorders genetic testing involves analyzing an individual's DNA to identify genetic mutations that could lead to birth defects or inherited conditions. This testing is often conducted before or during pregnancy to assess the risk of passing these disorders to the child. It can help parents make informed choices about their pregnancy and prepare for any health concerns. Additionally, it may provide valuable information for ongoing medical care for the child. By understanding these genetic factors, families can better navigate the challenges associated with congenital disorders.