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...