Tag: haemophilia and colour blindness

Questions Related to haemophilia and colour blindness

Melanin is found in.

  1. Whole skin

  2. Stratum spongiosum

  3. Stratum corneum

  4. Stratum germinativum


Correct Option: D

Mental retardation in children suffering from galactosemia can be avoided by

  1. Giving them more milk

  2. Giving them milk free diet

  3. Giving them milk fortified with vitamins

  4. Giving them more proteinous diet


Correct Option: B

Pigmentation of skin is due to.

  1. Melanocytes

  2. Leucocytes

  3. Lymphocytes

  4. Monocytes


Correct Option: A

Molecular probes are used for many genetic disorders like?

  1. Duchenne muscular dystrophy

  2. Cystic fibrosis

  3. Tay-Sachs disease

  4. All of these


Correct Option: A

Mark the correct statement.

  1. In lower one third part of oesophagus both Myenteric and Meissner's plexus are absent

  2. Carboxypeptidase is exopeptidase acting on 'N' terminal end of peptide chain

  3. Galactosemia is metabolic genetic disorder due to deficiency of the enzyme uridyl transferase

  4. Nucleotidase and nucleosidase enzymes are present in pancreatic juice


Correct Option: C
Explanation:
  • Here, option (C) is correct as Galactosemia is metabolic genetic metabolic disorder due to deficiency of the enzyme uridyl transferase.
  • While, carboxypeptidase is a protease enzyme that acts on 'C' terminal end of a protien or peptide.
  • And, in pancreatic juice trypsin, amylase and lipase are present.