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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


Team Careers360 16th Jan, 2024
Answer (1)
Team Careers360 21st Jan, 2024

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.

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