Match the human disorders shown in Group I with the biochemical processes in Group II. Choose the correct combination.
Group I | Group II |
P. Phenylketonuria | i. Melanin synthesis |
Q. Albinism | ii. Conversion of phenylalanine to tyrosine |
R. Homocystinuria | iii. Tyrosine degradation |
S. Argininemia | iv. Methionine metabolism |
v. Urea Synthesis |
Phenylketonuria - an autosomal recessive disorder causing absence of hydroxylase enzyme thus there is an inability of conversion of phenylalanine to tyrosine causing phenyl pyruvic idiocy and arthritis.
Albinism - an autosomal recessive condition causing tyrosinase deficiency. So, the melanin synthesis cannot take place.
Homocystinuria - a disorder of methionine metabolism causing abnormal deposition of homocysteine and its metabolites.
Argininimia - Autosomal recessive disorder. Due to deficiency of arginase enzyme, the arginine and ammonia get accumulated into the blood.
Thus matching all the options we find that correct answer is 'P-ii, Q-i, R-iv, S-v'.