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Newborn Screening

Newborn Screening

Description

Overview
Documentation

Newborn screening is screening test to identify infants at risk for the health disorders early enough to confirm the diagnosis.

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Overview

Newborn screening is a screening in infants shortly after birth for conditions that are treatable, but not clinically evident in the newborn period.

A small blood sample taken by pricking the baby’s heel, doctors can check for rare genetic, hormone-related, and metabolic conditions that can cause serious health problems with this simple blood test.

Newborn screening lets doctors diagnose babies quickly and start treatment as soon as possible.

Postnatal-SNP-microarray-01

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Documentation

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