Name: Babyshield 111, Urine-(LC)
Brand: Max Lab
SKU: 33410
Availability: InStock
Rating: 4.8 (4677 reviews)

How to book a Babyshield 111, Urine-(LC) at home near me?

You can easily book a Babyshield 111, Urine-(LC) with Max Lab by Max Hospitals. Just follow these simple steps:

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Select Babyshield 111, Urine-(LC) from the "Book a test" button or search from the search bar on the website or Max Lab App.

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Choose a convenient date and time slot for sample collection.

A trained and certified phlebotomist will visit your preferred location — home or office — at the scheduled time to collect your blood sample safely.

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The sample will be processed at the nearest Max Hospital or Max Laboratory, and your test reports will be delivered within the specified time.

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Swayam

The technician arrived right on time. The entire process felt clean and safe. Ideal for anyone who prefers testing from home!

Test Name :	Babyshield 111, Urine-(LC) Test
Sample Type :	NA
Gender :	Both
Age group :	All Age Groups
This 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 117 Tests

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Babyshield 111, Urine-(LC) Test