Newborn Screening tests in Dubai & UAE

Compare available Newborn Screening tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

1,200.00–3,000.00 AED

Clinical preparation

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Newborn Screening test prices

Showing 1–3 of 3 matching tests.

Newborn Screening diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2657 Comprehensive Newborn Screening Panel Test This test screens for over 50 inborn errors of metabolism using multiple analytical platforms.	Heel-prick capillary blood on filter paper (3 saturated spots)	Next day (samples Mon/Wed/Fri by 9 AM)	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Amino acid levels", "Acylcarnitine profiles", "Hormone markers", "Enzyme markers", "Hemoglobin variants"] Parameters [] Preparation ["Complete clinical details and comprehensive drug/supplement history must accompany the sample.", "Maternal medications (if breastfeeding) must be reported.", "Do not discontinue prescribed medications without consulting a physician."] Indications ["Routine newborn screening", "Screening for inherited metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 57732-8 ICD-10: Z13.21 Clinical summary This test screens for over 50 inborn errors of metabolism using multiple analytical platforms.
TEST-2681 Extended Newborn Screening Panel Test This diagnostic test evaluates a newborn's blood sample for over 50 inborn errors of metabolism, endocrine disorders, and hemoglobinopathies.	Dried Blood Spot (heel prick)	Next day (samples accepted Mon/Wed/Fri by 9 AM)	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Metabolic disorders", "Endocrine disorders", "Hemoglobinopathies"] Parameters [{"name": "Inborn Errors of Metabolism", "reference_range": "Detected via LC-MS/MS and immunoassays"}, {"name": "Endocrine Disorders", "reference_range": "Detected via LC-MS/MS and immunoassays"}, {"name": "Hemoglobinopathies", "reference_range": "Detected via LC-MS/MS and immunoassays"}] Preparation ["No specific fasting required", "Inform lab if baby is on TPN or antibiotics"] Indications ["Newborn screening", "Detection of inborn errors of metabolism", "Detection of endocrine disorders", "Detection of hemoglobinopathies"] Measurement technique Confirm with laboratory Codes LOINC: 73793-4 ICD-10: Z13.2 Clinical summary This diagnostic test evaluates a newborn's blood sample for over 50 inborn errors of metabolism, endocrine disorders, and hemoglobinopathies.
TEST-5990 Newborn Genetic Screening Panel (NGS) Test This diagnostic test evaluates DNA from a newborn's blood or FTA card to identify genetic variants associated with a wide range of inherited metabolic and genetic disorders.	Peripheral whole blood (heel prick or venipuncture) or FTA card	3–4 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in DNA", "Aminoacidopathies", "Organic acidurias", "Fatty acid oxidation defects", "Urea cycle disorders", "Lysosomal storage diseases"] Parameters [] Preparation [] Indications ["Screening for over 100 metabolic and genetic disorders in newborns", "Early detection and intervention for inherited conditions"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.89 Clinical summary This diagnostic test evaluates DNA from a newborn's blood or FTA card to identify genetic variants associated with a wide range of inherited metabolic and genetic disorders.

Category overview

Newborn Screening: overview

Welcoming a new baby is a joyous milestone, and proactively safeguarding their future health provides the ultimate peace of mind for your family. As a critical pediatric component of our Biochemistry services, comprehensive Newborn Screening evaluates a panel of crucial metabolic and genetic markers shortly after birth. Utilizing highly sensitive, state-of-the-art diagnostic technology, this early preventative testing helps identify rare congenital conditions before symptoms appear, safely guiding immediate, specialized medical care and dietary interventions. Widely trusted by pediatricians among premier diagnostic labs in the UAE, DNA Labs delivers absolute patient confidentiality, uncompromising diagnostic accuracy, and rapid reporting for time-sensitive results. Protect your baby’s lifelong well-being—book your newborn screening testing in UAE, coordinate a secure hospital or home sample collection, or consult our pediatric specialists.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.