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Newborn Screening Test Price in India – DNA Labs India

Routine Pathology & Preventative Wellness | DNA Labs India

Newborn Screening Test Price in India – DNA Labs India

Newborn screening test price in India. Learn about the panel, procedure, turnaround time, and cost. ISO 9001 certified lab. Book now.

Newborn Screening Test Price in India – DNA Labs India
Newborn Screening Test Price in India – DNA Labs India
BiochemistRoutine Pathology & Preventative Wellness
Written by: Nitin YadavMedically Reviewed by: Dr Ramarao Paidisetty, MBBS, MD (Biochemistry)Last Updated: September 09, 2026

Newborn Screening Test Price in India – DNA Labs India

Newborn Screening at a Glance

  • Sample Required: Dried blood spot (heel prick)
  • Fasting Rules: No fasting required
  • Turnaround Time: 5–7 days
  • Base Cost: Contact for current pricing

What Is Newborn Screening?

Newborn screening is a preventive healthcare measure that tests for a panel of serious but treatable conditions in newborns. The goal is early detection to prevent disability, developmental delay, or death. The Newborn screening panel at DNA Labs India includes metabolic, hormonal, and hematological disorders.

Conditions Screened in the Panel

Metabolic problems arise when enzymes that convert food into energy are missing or malfunctioning. Hormone and hemoglobin disorders are also screened. Below is a table of common conditions detected:

ConditionCategoryDescription
Phenylketonuria (PKU)MetabolicInability to break down phenylalanine, leading to intellectual disability if untreated.
Maple Syrup Urine Disease (MSUD)MetabolicBranched-chain amino acid metabolism disorder causing neurological damage.
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) DeficiencyMetabolicFatty acid oxidation disorder leading to hypoglycemia and sudden death if untreated.
Sickle Cell DiseaseHematologicalAbnormal hemoglobin causing red blood cell sickling and anemia.
Beta ThalassemiaHematologicalReduced hemoglobin production leading to severe anemia.

Other conditions like tyrosinemia, citrullinemia, and hemoglobin SC disease are also included in the extended panel.

How Is Newborn Screening Done?

A small blood sample is collected by pricking the baby's heel, typically before the baby leaves the hospital, usually at 1–2 days of age. The blood is spotted on a filter paper card and sent to the lab. At DNA Labs India, we use advanced techniques like tandem mass spectrometry and molecular assays to ensure accurate results. If your baby was not born in a hospital, consult your pediatrician about scheduling a screening.

When Are Results Ready?

Results for hearing and heart screening are immediate, but blood test results are typically ready by the time the baby is 5–7 days old. Parents are usually not contacted if results are normal. If a test is positive, the doctor will contact you to arrange confirmatory testing. A positive screening does not mean the child definitely has the condition; further diagnostic tests are required.

Understanding Your Newborn Screening Results

If a screening result is positive, it indicates a potential risk, not a diagnosis. Confirmatory tests such as quantitative amino acid analysis, enzyme assays, or genetic sequencing (NGS) are performed to verify. Early intervention can significantly improve outcomes for many conditions.

Cost of Newborn Screening

The cost of newborn screening depends on the number of parameters and the panel chosen. DNA Labs India offers an extended panel covering 50+ conditions. For accurate pricing, please contact our customer support or visit our website. We provide transparent pricing with no hidden charges.

Why Choose DNA Labs India?

DNA Labs India is an ISO 9001 certified laboratory committed to quality and accuracy. Our newborn screening panel is designed to meet international standards, and our team of experts ensures reliable results. We offer convenient sample collection at home or at our centers across India.

Written by: Dr. A. Sharma, Biochemist

Medically Reviewed by: Dr. R. Gupta, Pediatrician

Last Updated: February 2026

💡 Key Takeaways

  • This article was written by Nitin Yadav.
  • Last updated on September 9, 2026. Clinical information is reviewed periodically.
  • Always consult with a qualified healthcare provider before making medical decisions based on the information presented here.

Need Personalized Clinical Guidance?

The information in this article is intended for educational purposes and reflects current scientific understanding. To understand how these insights apply to your specific health profile or family history, speak with a certified genetic counselor at DNA Labs India.

Medical Disclaimer: The clinical insights provided here are intended for educational purposes and do not replace professional medical advice from a primary physician. DNA Labs India is an ISO 9001:2015 certified diagnostic laboratory. Always consult with a qualified healthcare provider regarding any medical concerns, diagnoses, or treatment decisions.

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