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Why we need New Born Screening

It's a First and foremost test to ensure baby's health. The purpose of NBS is the identification of a risk, certain genetic and metabolic abnormallities that cause specific disease that is preventable or treatable.

Benefits of the test

Detects over 70 hidden genetic and metabolic conditions that go unnoticed if not screened

Identification paves way to early intervention, treatment and prevention of disease progression

Recommended by W.H.O, already mandatory in several countries

New Born Screening

Test Test NameCurrencyAdd To Cart
FM-NBS-003Group C – Carnitine / Acylcarnitine Translocase Deficiency, 3-Hydroxy Long Chain Acyl-CoA Dehydrogenase Deficiency, Medium Chain Acyl-CoA Dehydrogenase Deficiency, Neonatal Carnitine Palmitoyl Transferase Deficiency Type II, Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Carnitine Palmitoyl Transferase Deficiency Type I1, 2,4-Dienoyl-CoA Reductase Deficiency1, Multiple Acyl-CoA Dehydrogenase Deficiency, Short-chain Acyl-CoA Dehydrogenase Deficiency, Trifunctional Protein Deficiency, Short chain Hydroxy Acyl-CoA Dehydrogenase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Glutaric Acidemia Type I, Isobutyryl-CoA Dehydrogenase Deficiency, Isovaleric Acidemia IVA, 2-Methylbutyryl-CoA Dehydrogenase Deficiency, 3-Methylcrotonyl-CoA Carboxylase Deficiency, 3-Methylglutaconyl-CoA Hydratase Deficiency, Methymalonyl-CoA Mutase Deficiency, Some Adenosylcobalamin Synthesis Defects CBL A,B/C,D, Maternal Vitamin B12 Deficiency, Mitochondrial Acetoacetyl-CoA Thiolase Deficiency BKT, Propionic Acidemia PROP, Multiple CoA Carboxylase Deficiency MCD, Malonic Aciduria, Argininemia, Argininosuccinic Aciduria, 5-Oxoprolinuria1 5-OXO, Carbamoylphosphate Synthetase Deficiency1, Citrullinemia CIT-I, Homocystinuria HCY, Hypermethioninemia MET, Hyperammonemia, Hyperornithinemia, Homocitrullinuria Syndrome1, Hyperornithinemia with Gyral Atrophy1 HOGA, Maple Syrup Urine Disease MSUD, Phenylketonuria PKU, Classical/Hyperphenylalaninemia, Biopterin Cofactor Deficiencies, Tyrosinemia TYR, Transient Neonatal Tyrosinemia, Tyrosinemia Type I1 TYR I, Tyrosinemia Type II TYR II, Tyrosinemia Type III TYR III, Hyperalimentation, Medium Chain Triglyceride Oil Administration, Treatment with Benzoate, Pyvalic Acid, or Valproic Acid, Liver Disease, Presence of EDTA Coagulants in Blood Specimen, Carnitine Uptake Deficiency, Congenital Hypothyroidism CH Group A, Galactosemia GAL, Congenital Adrenal Hyperplasia CAH, Glucose-6-Phosphate Dehydrogenase Deficiency G6PD, Biotinidase Deficiency BIO, Cystic Fibrosis CF, Sickle Cell Anemia Hb S/S, Sickle-C Disease Hb S/C, S-Beta Thalassemia Hb S/Th, Hb Variants

6,000.00 Add to cart