The Neonatal Screening Panel - 52+10 is a comprehensive health examination designed for newborns, offering an extensive assessment capable of detecting a broad spectrum of 62 different medical conditions. This non-invasive blood test utilizes a dried blood spot obtained through a simple heel-prick, with the collected sample undergoing Tandem Mass Spectrometry and other analytical procedures to pinpoint the presence of specific metabolic and genetic disorders.
Profile NameNeonatal Screening Panel - 52+10
Sample TypeDried Blood Spot
Preparations RequiredNo specific instructions required for this test.
Report Time6 days
This specialized neonatal screening panel, a blood test for newborns or a newborn screening panel, is paramount in identifying potential health conditions at the earliest stages, even before symptoms manifest. The utilization of advanced analytical techniques allows for the early detection of diseases such as Phenylketonuria (PKU), Galactosemia, Amino Acid, Organic Acid, and Fatty Acid Oxidation disorders, Congenital Hypothyroidism, Congenital Adrenal Hyperplasia, G6PD deficiency, Cystic Fibrosis, Sickle Cell Disease, Sickle Cell trait, Hb variants, and B thalassemia.
The primary objective of this screening panel is to facilitate prompt intervention and treatment, significantly enhancing a child’s long-term health outcomes and overall quality of life. Choose the Sprint Diagnostic Centre for precision and timeliness in your diagnosis.
Home Sample Collection Process
1
Book your convenient slot
2
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
4
Download Reports
Note: Home Sample Collection is only for Pathology lab tests.
Frequently Asked Questions
This panel can detect multiple serious and potentially life-threatening disorders in newborns, many of
which can be effectively treated if caught early. Early detection and treatment can dramatically improve
a child’s prognosis and quality of life.
No specific preparation is required. The test uses a dried blood spot sample, which is obtained through a
simple heel-prick procedure.
If your baby tests positive, it does not necessarily mean they have the condition. It means that further
tests are needed. Early detection allows for early intervention, which can significantly improve your
child’s long-term health outcomes.
The heel-prick procedure is generally safe and causes minimal discomfort to the baby. However, as with
any test, there may be a small risk of infection at the prick site.
Yes, the test can be performed on premature babies. However, depending on the baby's health condition,
the healthcare provider might decide the best time to take the sample.
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