Newborn Screening Report

Newborn ScreeningNewborn Screening report is a routine screening test that is performed shortly after birth to identify genetic disorders that can cause serious health problems if not detected and treated early. The report tests for a wide range of genetic disorders, including metabolic disorders, endocrine disorders, and hemoglobinopathies, among others.More than 1040 genes analyzed It is recommended if: This report is recommended for all newborns, as early detection and treatment can prevent or reduce the severity of many genetic disorders. Testing can provide valuable information to healthcare providers and parents, such as identifying infants who may need further testing or treatment. It can also provide reassurance for parents of unaffected infants. List of main conditions: Phenylketonuria Congenital hypothyroidism Galactosemia Sickle cell disease Cystic fibrosis Medium-chain acyl-CoA dehydrogenase deficiency Maple syrup urine disease Homocystinuria Biotinidase deficiency