In an individual with phenylketonuria,there i | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(C) Phenylketonuria $(PKU)$ is an inborn error of metabolism inherited as an autosomal recessive trait.In this disorder,the affected individual lacks

Vedclass · Accepted Answer

Tyrosine

Vedclass · Answer

(C) Phenylketonuria $(PKU)$ is an inborn error of metabolism inherited as an autosomal recessive trait.In this disorder,the affected individual lacks the enzyme phenylalanine hydroxylase.This enzyme is responsible for converting the amino acid phenylalanine into tyrosine.Due to the deficiency of this enzyme,phenylalanine accumulates and is converted into phenylpyruvic acid and other derivatives,which leads to mental retardation.

In an individual with phenylketonuria,there is an enzyme deficiency. This enzyme converts phenylalanine into ........ .

Similar Questions

Who is known as the father of human genetics?

In phenylketonuria:

$A$ normal-visioned man whose father was colourblind marries a normal woman whose father was also colourblind. They have one son. What is the probability of the son being colourblind (in $\%$)?

Give differences: Mendelian disorders and Chromosomal disorders.

If a color-blind woman marries a normal man,their offspring will be:

Vedclass Test Series

Exam Paper Generator

Online Exam Module