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

Related Mcqs:

1. Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?

   A. Parahydroxy phenyl pyruvate Hydroxylase
   B. Tyrosine transaminase
   C. Homogentisate oxidase
   D. Tyrosine oxidase

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

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

3. Scurvy is the result of deficiency of____________?

   A. Vitamin A
   B. Vitamin C
   C. Vitamin B
   D. Vitamin D

4. The 3 – D’s dermatitis, diarrhoea and dementia are seen in deficiency of____________?

   A. Thiamin
   B. Riboflavin
   C. Niacin
   D. Pyridoxine

5. Under metabolic conditions associated with a high rate of fatty acid oxidation liver produces________________?

   A. Glutamate
   B. Acetoacetate
   C. Cholesterol
   D. Glycine

6. During phagocytosis, the metabolic process called respiratory burst involves the activation of_____________?

   A. Oxidase
   B. Hydrolase
   C. Peroxidase
   D. Dehydrogenase

7. During phagocytosis the metabolic process called respiratory burst involves activation of_____________?

   A. Oxidase
   B. Hydrolase
   C. Peroxidase
   D. Dehydrogenase

8. Most importent compansatory mechanism in metabolic acidosis______________?

   A. Hyperventilation
   B. Increased NH3 excretion by kidneys
   C. Increased urinary phosphates
   D. Increased HCO3 Production

9. Acromegaly is a disorder of____________?

   A. Excess growth hormone secreting
   B. Excess thyroxine secretion
   C. Excess ACTH secretion
   D. Excess FSH secretion

10. Decreased basal metabolic rate is seen in_______________?

    A. Obesity
    B. Hyperthyroidism
    C. Feeding
    D. Exercise