Newborn Screening Panel 5 Test
Short Name: NBS Panel 5
Also known as: Congenital Hypothyroidism Screening, Galactosemia Test, PKU Test, Biotinidase Deficiency Test, Maple Syrup Urine Disease Test
Newborn Screening Panel 5 Test test available at DNA Labs India for ₹1,170. Uses Fluoroimmunoassay on Heel prick blood on filter paper samples. Results in Next day after sample receipt. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
The primary purpose of the Newborn Screening Panel 5 Test is to screen for specific genetic and metabolic disorders in newborns. It measures key parameters including Thyroid Stimulating Hormone (TSH) for congenital hypothyroidism, Glucose-6-Phosphate Dehydrogenase (G6PD) for G6PD deficiency, Biotinidase for biotinidase deficiency, and Phenylalanine for phenylketonuria (PKU). This early screening helps in identifying conditions that may not be visible at birth but can lead to serious health issues if untreated.
- Test Code
- 1299
- Price
- ₹1,170
- Sample Type
- Heel prick blood on filter paper
- Result Time
- Next day after sample receipt
- Fasting Required
- No
- Method
- Fluoroimmunoassay
Sample Collection
Clinical details and drug history must accompany the sample.
Method: Heel prick
Laboratory Analysis
A heel prick is performed to collect a few drops of blood on filter paper.
Report Delivery
The sample is properly stored and shipped to the laboratory for analysis.
Timeline: Next day after sample receipt
Patient Instructions
About This Test
Who Should Get This Test
The primary purpose of the Newborn Screening Panel 5 Test is to screen for specific genetic and metabolic disorders in newborns. It measures key parameters including Thyroid Stimulating Hormone (TSH) for congenital hypothyroidism, Glucose-6-Phosphate Dehydrogenase (G6PD) for G6PD deficiency, Biotinidase for biotinidase deficiency, and Phenylalanine for phenylketonuria (PKU). This early screening helps in identifying conditions that may not be visible at birth but can lead to serious health issues if untreated.
How to Prepare
- Collect 1 drop of heel prick blood on each of 3 spots on the filter paper provided.
- Ensure the filter paper is available from LPL.
- Ship the sample refrigerated or frozen.
- Include clinical details and drug history with the sample.
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"As a pediatrician, I recommend this test for all newborns to ensure early detection and management of metabolic disorders, promoting better health outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Sample not collected on proper filter paper
- Insufficient sample volume
- Sample stored improperly
Understanding Your Results
TSH
G6PD
Biotinidase
Phenylalanine
If the test results are abnormal or if the newborn shows any symptoms of the screened disorders, consult a pediatrician or genetic specialist immediately.
Limitations
- ⚠This is a screening test; positive results require confirmatory diagnostic testing
- ⚠May not detect all variants of the disorders
Risks & Considerations
- ●Minimal risk of slight discomfort or bruising at the heel prick site
- ●In rare cases, minor infection if not cared for properly
Interfering Factors
- ●Certain medications or supplements may affect results
- ●Improper sample collection or storage
Frequently Asked Questions
What is the Newborn Screening Panel 5 Test?
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What disorders does this test screen for?
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