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

More men suffer from colour blindness than women because

Red-green colour blindness appears due to

If both parents are carriers for thalassaemia,which is an autosomal recessive disorder,what are the chances of pregnancy resulting in an affected child?

If both parents are carriers for thalassemia,which is an autosomal recessive disorder,what are the chances of pregnancy resulting in an affected child?

If a mother is a carrier for colour blindness and the father is normal,then in the offspring,this disease may be seen in:

Vedclass Test Series

Exam Paper Generator

Online Exam Module