A newborn screening test is a common public health strategy that helps to diagnose several congenital disorders. It is usually done in 24 to 48 hours old of newborns. Newborn screening test includes phenylketonuria, sickle cell disease, congenital hypothyroidism, galactosemia, and homocystinuria.
Genetic Disorders in Children and Newborn Screening - An Overview
Early detection of genetic abnormalities through newborn screening allows prompt intervention to enhance affected children's health and quality of life.
Newborn Jaundice - After Discharge
Elevated blood bilirubin levels in infants are said to have newborn jaundice. Read further to know more.
Neonatal Hearing Screening: A Complete Guide for Little Ears
A newborn hearing screening test determines which newborns are most likely to have hearing loss and who need further assessment.
Neonatal Screening - An Important Aid to the Future of a Child
Neonatal screening includes tests done on the newborn to screen for various disorders. Read further to learn more.
