Question : Match the columns.
| Column-A (Disorder) | Column-B (Enzyme) |
| i. Gaucher disease | a. Phenylalanine hydroxylase |
| ii. Hunter syndrome | b. Hexosaminidase A |
| iii. Tay-Sachs disease | c. Iduronate-2-sulphatase |
| iv. Phenylketonuria | d. Glucocerebrosidase |
Option 1: i-a, ii-b, iii-c, iv-d
Option 2: i-b, ii-c, iii-a, iv-d
Option 3: i-d, ii-c, iii-b, iv-a
Option 4: i-b, ii-a, iii-d, iv-c
Correct Answer: i-d, ii-c, iii-b, iv-a
Solution : The correct options are i-d, ii-c, iii-b, and iv-a.
(i) Gaucher disease: Rare genetic disorder, lacks glucocerebrosidase enzyme.
(ii) Hunter syndrome: Mucopolysaccharidosis, lacks iduronate-2-sulfatase enzyme.
(iii) Tay-Sachs disease: Lysosomal storage disorder, lacks hexosaminidase A enzyme.
(iv) Phenylketonuria (PKU): Inherited metabolic disorder, lacks phenylalanine hydroxylase enzyme crucial for phenylalanine metabolism.
Related Questions
Question : Match Column-A with Column-B.
| Column-A (Vitamin) | Alternative name |
| i. Vitamin A | a. Ascorbic acid |
| ii. |
Question : Match the animals in column A with the phylum they belong to in column B
| Column-A | Column-B |
| i. Jelly Fish | a. |
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