Type II glycogen storage disorder is due to deficiency of______________?

Related Mcqs:

1. In which type of glycogen storage disease is hyper uricemia a feature ?

   A. I
   B. II
   C. III
   D. IV

2. Glycogen breakdown leads to formation of______________?

   A. Glucose
   B. Lactic acid
   C. Glucose & Lactic acid
   D. Glycoprotein

3. Alkaptonuria an inherited metabolic disorder is due to the deficiency of____________?

   A. Homogentisate oxidase
   B. Cystathionase
   C. Pheylalanine hydroxylase
   D. Tyrosine transaminase

4. Blood glucose level cannot be augmented by mobilization of muscle glycogen due to lack of_____________?

   A. G-6-P dehydrogenase
   B. G-6-P phydrogenase
   C. Aldolase
   D. Glucokinase

5. Beri-beri is caused due to the deficiency of______________?

   A. Thiamine
   B. Pyridoxine
   C. Ascorbic acid
   D. Riboflavin

6. Muscle glycogen, which cannot contribute to blood glucose due to the absence of which enzymes ?

   A. Phosphoglutamase
   B. Branching enzyme
   C. Debranching enzyme
   D. Glucose-6-phosphotase

7. Glycogen synthesis is increased by_____________?

   A. Cortisone
   B. Insulin
   C. GH
   D. Epinephrine

8. An essential for the conversion of glucose to glycogen in liver is____________?

   A. UTP
   B. GTP
   C. Pyruvate Kinase
   D. Guanosine

9. The tissue with the highest glycogen content (mg/100gm)_____________?

   A. Liver
   B. Muscle
   C. Kidneys
   D. Testes

10. Number of ATP molecules generated in the conversion of glycogen of lactate is_____________?

    A. 2
    B. 36
    C. 38
    D. 32