Max Lab > Lab Test in Amritsar > Lab Test in Pratapnagar > Baby Shield TMS 62 Test (LC)
Test Type:
NA
Test Includes:
Congential Hypothyroidism, G6PD Deficiency (G6PD), Biotinidase deficiency, Congenital Adrenal Hyperplasia (17-OHP), Congenital Hypothyroidism (TSH), Cystic Fibrosis, Galactosemia, Sickle Cell Anaemia (Hb SS), Beta thalassemia, Sickle Cell Disease, Variant hemoglobinopathies(C.D,H, bart band) including Hb E(Var Hb), Amino acid Disorders, Argininemia ARG, Argininosuccinic aciduria, 5-oxoprolinuria, carbamoyl phosphate synthetase 1- deficiency, Citrullinenia CIT-I, Homocystinuria, Hypermethioninemia, Hyperornithinemia-hyperammoninemia-hyperhomocitrullinemia (HHH) syndrome, Hyperornithinemia with Gyral Atrophy 1 HOGA, Maple syrup urine disease (MSUD), Classical Hyperphenylalaninemia, Transient neonatal tyrosinemia, Tyrosinemia Type 1, Tyrosinemia Type II, Tyrosinemia Type III, Ornithine transcarbamylase deficiency, Citrullinemia type II, Biopterin defect in cofactor biosynthesis BIOPT (BS), Bioptrin defect in confactor regeneration BIOPT (REG), Fatty Acid Oxidation and Other Disorders, Carnitine Acylcarnitine Translocase Deficiency CACT, 3-Hydroxy Long Chain Acyl-CoA Dehydrogenase Deficiency LCHAD, Medium chain acyl CoA dehydrogenase deficiency, Neonatal Carnitine Palmitoyl Transferase Deficiency Type II CPT-II, Very Long Chain Acyl-CoA Dehydrogenase Deficiency VLCAD, Carnitine Palnitoyl Transferase Deficiency Type II CPT-I, 2,4-Dienoyl-CoA Reductase Deficiencyl DE-RED, Multiple Acyl-CoA Dehydrogenase Deficeincy GA-II, Short chain acyl CoA dehydrogenase deficiency, Trifunctional Protein Deficiency TFP , Short chain Hydroxy Acyl-CoA Dehydrogenase Deficiency SCHAD, 3-Hydroxy-3-Methylglutary-CoA Lyase Deficiency HMG, Gluatric Acidemia Type 1 GA-1, Isobutyryl-CoA dehydrogenase deficiency (IBD), Isovaleric acidemia, 2-Methylbutyryl-CoA Dehydrogenase Deficiency 2MBG, 3-Methylcrotonyl-CoA Carboxylase Deficiency 3MCC, 3-Methylglutaconyl-CoA Hydratase Deficiency 3MGA, Methymalonyl-CoA Mutase Deficiency MUT, Maternal Vitamin B12 Deficiency, Mitochondrial Acetoacetyl-CoA Thiolase Deficiency BKT, Propionic acidemia, Multiple CoA Carboxylase Deficiency MCD, Malonic acidemia (MAL), Hyperalimentation, Medium Chain Triglyceride Oil Administration MCT, Treatment with benzoate, Pyvalic Acid, or Valproic Acid, Liver Disease, Presence of EDTA Coagulants in Blood Specimen, Carnitine Uptake Deficiency CUD, Medium-chain ketoacyl-CoA thiolase deficiency MCAT, Methylmalonic Acidemia ( Cobalamin disorders) Cbl A, B, Methylmalonic Acidemia with homocystinuria Cbl C, D
Test Price:
₹ 4990
Baby Shield TMS 62 Test (LC) Price |
₹ 4990
|
Test booked so far
Test Recommended for: Both
Recommended for age: All Age Groups
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