ALL ABOUT
NEWBORN SCREENING
Newborn Screening is the practice of testing all babies in their first days of life for certain disorders and conditions that can hinder their normal development. This testing is required in every state and is typically performed before the baby leaves the hospital. Early detection and treatment can prevent intellectual and physical disabilities and lifethreatening illnesses.
HOW & WHEN The newborn screening usually begins with a blood test 24 to 48 hours after a baby is born, while he or she is still in the hospital. This test is performed by pricking the baby’s heel to collect a few drops of blood. In newborn screening, the baby will be tested for the following family inherited and hormonal problems.
It includes
Phenylketonuria, Congenital Hypothyroidism, Congenital Adrenal Hyperplasia, Sickle cell disease, Thalassemia, Galactosemia, Biotinidase, Cystic Fibrosis, Hearing Loss.
If the test result was positive, this does not necessarily mean that your baby has any of these health problems. This test only finds babies that are at increased risk for these health problems. More testing and examination by specialists are then usually required to find out if the disorder is present. The extra testing is important because early diagnosis and treatment can prevent many health-related problems.
The treatment for each condition is different. Treatment may include a special diet, hormones and or medications. If your baby has one of these conditions, it is very important to start the treatment as soon as possible.
To know more about newborn screening Dubai visit: https://www.fml-dubai.com/metabolic-screening-tests/