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Babyshield 111, Urine-(LC) Test

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
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Babyshield 111, Urine-(LC) Test

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Babyshield 111, Urine-(NE) Test Price in Other Cities

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Babyshield 111, Urine-(LC) Test

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RECOMMENDED PACKAGES

CBC (Complete Blood Count) Test

CBNAAT Covid 19 Assay Test

Covid-19 RT PCR Test in Delhi

Dengue NS 1 Antigen Test

Covid-19 RT PCR Test in Haryana

Covid-19 RT PCR Test in Uttar Pradesh

Covid 19 IgG Antibody (Quantitative) Test

Thyroid Stimulating Hormone (TSH) Test

HbA1c, Glycated Hemoglobin Test

Creatinine Test

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Bilirubin Total and Direct Test

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Vitamin B12 Test

IgE (Immunoglobulin-E) Test

SARS-COV-2 Spike Antibodies Test

Double Marker Test

Free PSA (Prostate Specific Antigen) Test

Allergy Screen-PhadiaTop/Inf Test

Triglycerides Test

Allergy Comprehensive Test

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