Newborn Screening is a program that identifies babies at risk of having rare, but serious medical conditions that can affect normal development. BabyShield Newborn Screening combines biochemical testing of 100+ metabolic & genetic conditions with confirmatory genetic testing for screen-positive results. It aims to achieve early identification of conditions. This results in early intervention that can lead to the elimination or reduction of mortality, morbidity, and disability in affected newborns. Early Diagnosis of disease - Reflex genetic testing to screen for positive conditions helps in the identification of genetic anomalies that can help make a quick diagnosis. Faster Initiation of Treatment: Confirmation of a screened positive result with reflex genetic testing within 96 hours helps ensure prompt treatment and effective disease management. Between 48-72 hours after birth, your physician, nurse or a trained member of the hospital staff will collect a urine sample or a few drops of blood onto a screening card by pricking your baby’s heel.
FOR MORE DETAILS YOU CAN CONTACT US ON 7506692725.
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