Newborn Screening Panel Comprehensive Test
Also known as: Neonatal Screening Panel, Newborn Metabolic Screening
Newborn Screening Panel Comprehensive Test test available at DNA Labs India for ₹7,500. Uses Fluoroimmunoassay, Capillary Electrophoresis, Tandem Mass Spectrometry on 1 drop of heel prick blood each on 3 spots of filter paper samples. Results in Report available next day after sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification improves long-term prognosis, minimizes complications, and identifies families for genetic counseling.
- Test Code
- 1301
- Price
- ₹7,500
- Sample Type
- 1 drop of heel prick blood each on 3 spots of filter paper
- Result Time
- Report available next day after sample receipt.
- Fasting Required
- No
- Method
- Fluoroimmunoassay, Capillary Electrophoresis, Tandem Mass Spectrometry
Sample Collection
Ensure the newborn is calm and warm. No special preparation needed, but clinical details and drug history must accompany the sample.
Method: Heel prick
Laboratory Analysis
Heel prick is performed by a trained professional to collect blood drops on filter paper. The process is quick and minimally invasive.
Report Delivery
Apply gentle pressure to the heel to stop bleeding. Store the filter paper sample as instructed.
Timeline: Report available next day after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification improves long-term prognosis, minimizes complications, and identifies families for genetic counseling.
How to Prepare
- Use filter paper provided by LPL
- Apply blood to designated spots
- Store at room temperature for up to 2 hours, refrigerate for up to 1 week
- Do not freeze the sample
- Include clinical details and drug history with the sample
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early newborn screening is crucial for detecting treatable genetic disorders, allowing for timely intervention and improved long-term health outcomes for infants. Consult with your healthcare provider to schedule this test."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Improperly labeled or contaminated sample
- Sample stored beyond stability period
Understanding Your Results
Consult a doctor if the test result is positive or if the newborn shows symptoms such as poor feeding, jaundice, or seizures.
Limitations
- ⚠False positives or negatives may occur
- ⚠Does not cover all possible genetic disorders
- ⚠Confirmatory testing required for positive results
Risks & Considerations
- ●Minor bruising or discomfort at the heel prick site
- ●Rare risk of infection at the collection site
Interfering Factors
- ●Improper sample collection or handling
- ●Contamination of filter paper
- ●Recent blood transfusion
- ●Delayed sample submission
Frequently Asked Questions
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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