Q. Individuals suffering from phenylketonuria lack an enzyme required for the conversion of

 165  165 NTA AbhyasNTA Abhyas 2022 Report Error

Solution:

Phenylketonuria is an autosomal recessive disorder. The affected individual lacks an enzyme that converts the amino acid phenylalanine into tyrosine. As a result of this phenylalanine is accumulated and converted into phenylpyruvic acid and other derivatives. Accumulation of these in brain results in mental retardation. These are also excreted through urine because of its poor absorption by the kidney.