Newborn Screening Tests – How it Help Identify the Birth Defects

  • Request a call back
Newborn Screening Tests – How it Help Identify the Birth Defects

Just how do birth defects happen? What can be done to identify birth defects? How do I make sure that my baby comes away healthy and safe? Ahead of getting pregnant, it is crucial that you take time to realize why and how exactly birth defects happen. It becomes even more important that you learn the ways to prevent birth abnormalities.

By the time a woman gets pregnant, there is a slight chance that her baby will have a birth defect. On average, 96-97 percent of infants are born healthy. The 3-4 percent is the quantity estimated as the rate for birth defects.

Listing here disorders those usually included in newborn screening programs:

Phenylketonuria (PKU) – Identify metabolism disorders in newborns.

Sickle cell disease - A blood disorder in which red blood cells are not able to move through the blood stream.

Cystic fibrosis (CF) – It is a genetic disorder that affects newborn lungs and digestive system.

Severe combined immunodeficiency (SCID) – It is a severe immune system disorder that make is impossible your immune system to fight with infections, viruses, and bacteria.

Hearing aids – Make sure your newborn get screened for hearing test within the first 3 weeks of life.

Right now there are a variety of tests which is often considered by the parent of a newborn. All these can help lessen your risks of giving birth to a baby with a birth defect. Further ask your doctor what suits you best.