OROTIC ACIDURIA- Pyrimidine disorder

OROTIC ACIDURIA- Pyrimidine disorder

Orotic aciduria Q. 1 Orotic aciduria is due to deficiency of ‑  A Decarboxylase  B Tyrosinase  C Isomerase  D Homogentisate oxidase Q. 1 Orotic aciduria is due to deficiency of ‑  A Decarboxylase  B Tyrosinase  C Isomerase  D Homogentisate oxidase Ans. A Explanation: Ans. is ‘a’ i.e., Decarboxylase  Metabolic disease Enzyme deficient Maple syrup urine […]

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OROTIC ACIDURIA- Pyrimidine disorder

OROTIC ACIDURIA- Pyrimidine disorder OROTIC ACIDURIA It is a rare autosomal recessive condition. It is due to the deficiency of UMP synthase, a bifunctional enzyme having- Orotate phosphoribosyl transferase Orotic acid decarboxylase (orotidylate decarboxylase) It is characterized by excretion of uric acid in urine. Two types- Type I oroctic aciduria- deficiency of orotate phosphoribosyl transferase

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