With respect to phenylketonuria,identify whic | vedclass

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

Question

(A) is the correct answer because it is not a case of aneuploidy.$1$. Phenylketonuria $(PKU)$ is an inborn error of metabolism.$2$. It is an autosomal

Vedclass · Accepted Answer

It is a case of aneuploidy

Vedclass · Answer

(A) is the correct answer because it is not a case of aneuploidy.$1$. Phenylketonuria $(PKU)$ is an inborn error of metabolism.$2$. It is an autosomal recessive disorder caused by a mutation in the gene encoding the enzyme phenylalanine hydroxylase.$3$. This enzyme is required to convert the amino acid phenylalanine into tyrosine in the liver.$4$. Because the defective gene affects multiple phenotypic traits (such as mental retardation and reduction in hair and skin pigmentation),it is a classic example of pleiotropy.

With respect to phenylketonuria,identify which statement is not correct.

Similar Questions

Wilson detected the colour blindness disease in

Given below is a pedigree chart of a family with five children. It shows the inheritance of attached earlobes as opposed to the free ones. The squares represent the male individuals and circles the female individuals. Which one of the following conclusions drawn is correct?

In sickle-cell anaemia,which of the following amino acids is substituted?

Which of the following is an example of qualitative inheritance?

Which statement is correct regarding the inheritance of an autosome-linked recessive gene?

Vedclass Test Series

Exam Paper Generator

Online Exam Module