Histochemical demonstration of glycogen in the cells can help in the diagnosis of_________________?

Related Mcqs:

1. A 3-year old child presented with progressive anaemia, jaundice & failure to thrive. O/E: pallor, splenomegaly are seen Peripheral smear showed normoblasts and small round intensely stained red cells. The likely diagnosis is________________?

   A. Here ditary spherocytosis B. Thalassaemia C. Sickle cell anaemia D. Vitamin B12 deficiency anaemia...

2. A child’s CSF was examined I contains slightly raised or normal PMN cells, raised lymphocytes, absence of mycotic growth, value of protein is normal or above normal, glucose level is normal. The most probable diagnosis is____________?

   A. Pyogenic bacterial meningitis B. Viral meningitis C. Fungal meningitis D. Tuberculous meningitis...

3. Frozen sections can be used for the demonstration of_____________?

   A. Fat B. Mucin C. Cartilage D. Iron...

4. Stain used for demonstration of amyloid is______________?

   A. Congo Red B. Masson’s toichrome C. Vonkosa D. Reticulin...

5. 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...

6. Muscle glycogen cannot contribute directly to blood glucose level because___________?

   A. Muscle lacks glucose 6 phosphatase B. Muscle lacks phospho gluco isomerase C. Absence of glucokinase D. Muscle does not contain glycogen phosphorylase...

7. Glycogen synthesis is increased by_____________?

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

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

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

9. Glycogen breakdown leads to formation of______________?

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

10. Type II glycogen storage disorder is due to deficiency of______________?

    A. Alpha -Glucosidase B. Alpha galactosidase C. Muscle phosphorylase D. Acid Lipase...