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DNA Labs India

Newborn Screening Panel 4 Test

DNA Labs India | ISO 9001:2015 Certified

Newborn Screening Panel 4 Test

Short Name: Newborn Screening Panel 4

Newborn Screening Panel 4 Test test available at DNA Labs India for ₹1,170. Uses Fluoroimmunoassay on Heel prick blood spots on filter paper samples. Results in Next day if sample received Monday through Friday by 9 am.. Free home collection in 300+ cities across India.

Blood TestNeonates (0-28 days)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Newborn Screening Panel 4 Test is to detect four specific conditions in newborns: Thyroid disease (measured via TSH), G6PD deficiency, Congenital Adrenal Hyperplasia (measured via 17-Hydroxyprogesterone), and Galactosemia (measured via Total Galactose). Early identification enables prompt treatment to prevent serious health issues.

Test Code
1296
Price
₹1,170
Sample Type
Heel prick blood spots on filter paper
Result Time
Next day if sample received Monday through Friday by 9 am.
Fasting Required
No
Method
Fluoroimmunoassay
Step 1

Sample Collection

Ensure the infant is comfortable and calm. Have clinical details and drug history ready to accompany the sample.

Method: Heel prick

Step 2

Laboratory Analysis

A healthcare professional will perform a heel prick on the newborn to collect blood spots on the designated filter paper card.

Step 3

Report Delivery

Apply gentle pressure to the heel to stop bleeding. Store the sample as per instructions and send it to the lab promptly.

Timeline: Next day if sample received Monday through Friday by 9 am.

Patient Instructions

1
Before the Test:No specific preparation is required, but ensure clinical details and drug history are available.
2
During the Test:The test involves a quick heel prick to collect blood spots on filter paper, causing minimal discomfort.
3
After the Test:The heel may be slightly sore; apply gentle pressure if needed. Results will be available next day if sample received by 9 am Mon-Fri.

About This Test

Who Should Get This Test

The purpose of the Newborn Screening Panel 4 Test is to detect four specific conditions in newborns: Thyroid disease (measured via TSH), G6PD deficiency, Congenital Adrenal Hyperplasia (measured via 17-Hydroxyprogesterone), and Galactosemia (measured via Total Galactose). Early identification enables prompt treatment to prevent serious health issues.

How to Prepare

  • Collect 1 drop of heel prick blood each on 3 spots of filter paper available from LPL.
  • Ship the sample refrigerated or frozen.
  • Clinical details and drug history must accompany the sample.

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeHeel prick blood spots on filter paper
Sample VolumeFew drops of blood
ContainerFilter paper card
Collection MethodHeel prick

Sample Stability

Room Temperature: 2 hours
Refrigerator: 1 week
Frozen: 1 week

Understanding Your Results

If the test results are abnormal, further testing may be required to confirm the diagnosis. It is important to follow up with a healthcare provider to discuss the test results and any necessary treatment.
Abnormal TSH levels may indicate congenital hypothyroidism.
Low G-6PD levels may suggest G6PD deficiency.
Elevated 17-Hydroxyprogesterone may point to Congenital Adrenal Hyperplasia.
High Total Galactose levels may indicate galactosemia.
Results outside normal ranges require clinical correlation and confirmatory testing.
⚠️ When to Consult a Doctor:

Consult a healthcare provider immediately if test results are abnormal or if the newborn shows symptoms like poor feeding, lethargy, jaundice, or frequent infections.

Risks & Considerations

  • Minimal risk of slight bruising or discomfort at the heel prick site

Frequently Asked Questions

What is the Newborn Screening Panel 4 Test?
It is a blood test that screens newborns for four conditions: congenital hypothyroidism, cystic fibrosis, galactosemia, and phenylketonuria (PKU).
Why is this test important for newborns?
Early detection through screening allows for timely treatment, preventing serious health complications and ensuring better long-term outcomes.
What conditions does this test screen for?
It screens for congenital hypothyroidism, cystic fibrosis, galactosemia, and phenylketonuria (PKU).
How is the test performed?
A small blood sample is collected via heel prick and placed on filter paper for analysis using fluoroimmunoassay.
What is the cost of the test?
The cost is INR 1170 at DNA Labs India, with free home sample collection available.
Is home sample collection available?
Yes, free home collection is offered for online bookings across many cities in India.
How long does it take to get the results?
Results are typically available the next day if the sample is received Monday to Friday by 9 am.
What if the test results are abnormal?
Abnormal results require follow-up with a healthcare provider for confirmatory testing and treatment planning.
Are there any risks associated with the test?
The test is safe with minimal risks, such as slight bruising at the heel prick site.
Do I need to fast before the test?
No fasting is required, but clinical details and drug history should be provided.
What should I bring to the appointment?
Bring any relevant medical history and ensure the newborn is comfortable for the procedure.
How can I book the test?
You can book online through DNA Labs India's website or contact them directly for appointment scheduling.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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