Biology, asked by nivekitty6386, 1 year ago

Phenylketonuria is caused by defect in what metabolism?

Answers

Answered by Anonymous
1
phenylketonuria is an inherited condition caused by a defect in the PAH gene. The PAH gene helps create phenylalanine hydroxylase, the enzyme responsible for breaking down phenylalanine. A dangerous buildup of phenylalanine can occur when someone eats high-protein foods, such as eggs and meat.
Answered by limelight1726
5

Explanation:

Phenylketonuria is a autosomal mendelian disorder .

It is due to recessive gene on chromosome No - 12 .

It accumulate in nerve cells of brain and hence lead to the mental retardation

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