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