Newborn Screening Panel 8 Test
Short Name: NBS Panel 8 Test
Also known as: Newborn Screening Test, NBS-8, Metabolic Screening Panel
Newborn Screening Panel 8 Test test available at DNA Labs India for ₹3,000. Uses Fluoroimmunoassay, Capillary Electrophoresis on Heel prick blood samples. Results in Results are typically available within 24-48 hours 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 purpose of the Newborn Screening Panel 8 Test is to identify newborns who may have certain metabolic, endocrine, or genetic disorders. Early identification enables prompt treatment, which can prevent severe health consequences, improve long-term prognosis, and reduce infant morbidity and mortality.
- Test Code
- 1310
- Price
- ₹3,000
- Sample Type
- Heel prick blood
- Result Time
- Results are typically available within 24-48 hours after sample receipt.
- Fasting Required
- No
- Method
- Fluoroimmunoassay, Capillary Electrophoresis
Sample Collection
Ensure the baby is calm and comfortable. Clean the heel area with antiseptic and allow it to dry.
Method: Heel prick
Laboratory Analysis
A healthcare provider will perform a heel prick to collect small blood drops onto filter paper cards.
Report Delivery
Apply gentle pressure to the heel to stop bleeding. Keep the sample refrigerated and ship as per instructions.
Timeline: Results are typically available within 24-48 hours after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Newborn Screening Panel 8 Test is to identify newborns who may have certain metabolic, endocrine, or genetic disorders. Early identification enables prompt treatment, which can prevent severe health consequences, improve long-term prognosis, and reduce infant morbidity and mortality.
How to Prepare
- Sample type: 1 drop of heel prick blood each on 3 spots of filter paper
- Ship refrigerated, do not freeze
- 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
"Newborn screening is vital for early detection of treatable disorders, ensuring timely intervention and better outcomes for infants."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Incorrect sample collection technique
- Contaminated or insufficient sample
- Missing clinical details
- Sample not stored or shipped correctly
Understanding Your Results
Phenylketonuria (PKU)
Congenital Hypothyroidism (CH)
Biotinidase deficiency
Galactosemia
G6PD deficiency
Hemoglobinopathies
Cystic Fibrosis
Maple Syrup Urine Disease (MSUD)
If your baby shows symptoms such as developmental delays, poor feeding, vomiting, jaundice, seizures, or low muscle tone, consult a healthcare provider immediately.
Limitations
- ⚠This is a screening test; positive results require confirmatory testing
- ⚠May not detect all variants or mild forms of disorders
- ⚠False positives or negatives can occur
- ⚠Does not cover all possible genetic conditions
Risks & Considerations
- ●Minimal risk from heel prick, such as slight bruising or discomfort
- ●Rare chance of infection if not performed aseptically
Interfering Factors
- ●Premature birth may affect results
- ●Recent blood transfusion
- ●Dietary factors or supplements
- ●Medications affecting metabolism
- ●Contaminated sample
Compare With Similar Tests
| Test | Newborn Screening Panel 8 Test | Expanded Newborn Screening Panel | Basic Newborn Screening | Genetic Carrier Screening |
|---|---|---|---|---|
| Comparison | Newborn Screening Panel 8 Test |
Frequently Asked Questions
What is the Newborn Screening Panel 8 Test?
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