Newborn Screening Panel Basic Test
Short Name: Newborn Screening Basic
Also known as: Newborn Blood Spot Screening, NBS Basic Panel
Newborn Screening Panel Basic Test test available at DNA Labs India for ₹1,638. Uses Fluoroimmunoassay, Capillary Electrophoresis on Heel prick blood on filter paper samples. Results in Next day after sample receipt if collected by 9 am on Mon, Wed, or Fri.. 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
This test screens for: TSH (thyroid-stimulating hormone) to detect thyroid disorders, 17-Hydroxyprogesterone for congenital adrenal hyperplasia, G6PD (glucose-6-phosphate dehydrogenase) for enzyme deficiency, and Hemoglobinopathy for blood disorders like sickle cell disease.
- Test Code
- 1300
- Price
- ₹1,638
- Sample Type
- Heel prick blood on filter paper
- Result Time
- Next day after sample receipt if collected by 9 am on Mon, Wed, or Fri.
- Fasting Required
- No
- Method
- Fluoroimmunoassay, Capillary Electrophoresis
Sample Collection
No special preparation required
Method: Heel prick
Laboratory Analysis
Heel prick procedure performed by a trained professional
Report Delivery
Apply gentle pressure to stop bleeding and keep the area clean
Timeline: Next day after sample receipt if collected by 9 am on Mon, Wed, or Fri.
Patient Instructions
About This Test
Who Should Get This Test
This test screens for: TSH (thyroid-stimulating hormone) to detect thyroid disorders, 17-Hydroxyprogesterone for congenital adrenal hyperplasia, G6PD (glucose-6-phosphate dehydrogenase) for enzyme deficiency, and Hemoglobinopathy for blood disorders like sickle cell disease.
How to Prepare
- Collect 1 drop of blood on each of 3 filter paper spots
- Ship sample refrigerated or frozen
- 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 vital for identifying treatable genetic conditions before symptoms manifest, allowing for timely intervention and improved outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Contaminated or damaged filter paper
- Missing clinical information or consent
Understanding Your Results
TSH
17-Hydroxyprogesterone
G6PD
Hemoglobinopathy
If results are abnormal or if the child shows symptoms such as poor feeding, jaundice, or developmental delays.
Limitations
- ⚠False positive/negative results possible
- ⚠Not a diagnostic test; confirmatory testing may be needed
- ⚠Limited to specific disorders in the panel
Risks & Considerations
- ●Minor bruising at the heel prick site
- ●Small risk of infection at the puncture site
- ●Temporary discomfort for the newborn
Interfering Factors
- ●Improper sample collection
- ●Contamination of filter paper
- ●Premature birth affecting results
Compare With Similar Tests
| Test | Newborn Screening Panel Basic Test | Newborn Screening Panel Advanced | Individual Genetic Tests |
|---|---|---|---|
| Comparison | Newborn Screening Panel Basic Test |
Frequently Asked Questions
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