Max Lab > Lab Test in Sonipat > Lab Test in Jatheri > Babyshield 111, Urine-(LC) Test
Test Type:
NA
Test Includes:
Amino Acidopathies and Organic Acidemias:, Beta-ketothiolase deficiency (BKT), Alkaptonuria, Argininemia, Biotinidase deficiency, carbamoyl phosphate synthetase 1- deficiency, Dihydrolipoyl dehydrogenase(E3) deficiency, Familial Renal iminoglycinuria, Glutaric aciduria type I, Glutaric aciduria type II, Hartnup Disease, Homocystinuria, Hyperhydroxyprolinemia, 3-hydroxy-3-methylglutaryl-CoA-lyase deficiency, Hyperleucine-isoleucinemia, Iminoglycinuria, Isovaleric acidemia, 2-ketoadipic aciduria, Lysinuric protein intolerance, Maple syrup urine disease (MSUD), 3-methylcrotonyl CoA carboxylase deficiency, 3-methylglutaconic aciduria, Methylmalonic semialdehyde dehydrogenase deficiency, Mevalonic aciduria, Ornithine transcarbamylase deficiency, Phenylketonuria (PKU), Propionic acidemia, Transient neonatal tyrosinemia, Tyrosinemia Type 1, Valinemia, Canavan disease, Multiple carboxylase deficiency, Hyperglycinuria(non-ketotic), Hypersarcosinemia, Hypermethioninemia, Argininosuccinic aciduria, Citrullinemia Type 1, Cystathioninuria, Hyperornithinemia-hyperammoninemia-hyperhomocitrullinemia (HHH) syndrome, Hyperprolinemia type I, Hyperprolinemia type II, Saccharopinuria, Tyrosinemia Type II, Tyrosinemia Type III, Xanthurenic aciduria, Formiminoglutamic aciduria, Glutathionuria, Histidinemia, Serum carnosinase deficiency, Histidinuria, Hydroxylysinuria, Tryptophanuria with dwarfism, beta-aminoisobutyric aciduria, Hyperpipecolatemia, Imidazole amino aciduria, Hyperglycinuria (ketotic), 3-hydroxyisobutyryl CoA deacylase deficiency, Defects of biopterin cofactor biosynthesis (BIOPT BS), Defects of biopterin cofactor regeneration (BIOPT REG), NICCD, Benign hyperpheny lalaninemia, Cystinuria, Citrullinemia type II, Methylmalonic acidemia (MMA) - Cbl C, D, Malonic acidemia (MAL), Methylmalonic aciduria cblA and cblB forms (MMA, Cbl A,B), Methylmalony-CoA mutase deficiency (MUT), Isobutyryl-CoA dehydrogenase deficiency (IBD), Aminoacylase I Deficiency, Succinic semialdehyde dehydrogenase deficiency, Hawkinsunuria, Lysinuria, N-acetylglutamate / Carbamylphosphate synthetase deficiency, 5-oxoprolinuria, Tyrosinemia caused by liver dysfunction, TCA Cycle/Mitochondrial Abnormality:, Fumarate hydratase deficiency, Pyruvate carboxylase deficiency, Pyruvate decarboxy deficiency, Pyruvate dehydrogenase ( EI ) deficiency, Pyruvate dehydrogenase phosphatase deficiency, Leigh syndrome, Disorders of Fatty Acid Metabolism, Medium chain acyl CoA dehydrogenase deficiency, Short chain acyl CoA dehydrogenase deficiency, Ethyl Malonic Aciduria, Mitochondrial trifunctional protein Deficiency, Glycerol Kinase Deficiency, Peroxisomal Disorders, Zellweger like syndrome, Zellweger syndrome, Primary hyperoxaluria type 2, Infantile refsum disease, Neonatal Adrenoleukodystrophy, Primary hyperoxaluria Type I, Disorders of Purine and Pyrimidine Metabolism, Lesch-Nyhan syndrome, Dihydropyrimidinase Deficiency, Orotic aciduria, Thymine Uraciluria, Xanthinuria, Adenosine deaminase deficiency, Adenine phosphoribosyl transferase deficiency, Partial deficiency of hypoxanthine-guanine phosphoribosy Itransferase deficiency, Hyperuric acidemia, Disorders of Sugars :, Fructose-I and 6-diphosphatase deficiency, Galactosemia, Endogenous sucrosuria, D-glyceric aciduria, Lactose Intolerance, Galactokinase deficiency (GALK), Galactose epimerase deficiency (GALE), Fructosamine, Transient Galactosemia, Non-IEM Disorder:, Neuroblastoma
Test Price:
₹ 3500
Babyshield 111, Urine-(LC) Test Price |
₹ 3500
|
Test booked so far
Test Recommended for: Both
Recommended for age: All Age Groups
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