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

Related Mcqs:

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

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

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

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

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

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

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. Ketone bodies are by products of metabolism of_____________?

   A. Carbohydrate
   B. Protein
   C. Fat
   D. All of the above

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

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

7. Most importent compansatory mechanism in metabolic acidosis______________?

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

8. Amelogenesis imperfecta is a disorder of_____________?

   A. Ectoderm
   B. Mesoderm
   C. Endoderm
   D. Ecto and Mesoderm

9. Decreased basal metabolic rate is seen in_______________?

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

10. Basic metabolic unit of bone is_______________?

    A. Osteon
    B. Osteoblast
    C. Osteocyte
    D. Osteoclast