Biology, asked by alishaabraham, 1 year ago

give the symptoms of phenyl ketonuria....

Answers

Answered by Anonymous
2

Phenylketonuria is a genetic disorder which is autosomal recessive...

It's symptoms are...
✴️Retarded mental growth
✴️Presence of ketone body in urine ...

Hope it helps !! ❤️✌️


Anonymous: :) no prob.
Answered by TheInnocentSoul
0

Hey mate ☺️

 \huge \red {Ur Answer}

Phenylketonuria (fen-ul-key-toe-NU-ree-uh), also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is caused by a defect in the gene that helps create the enzyme needed to break down phenylalanine.

Phenylketonuria (fen-ul-key-toe-NU-ree-uh), also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is caused by a defect in the gene that helps create the enzyme needed to break down phenylalanine.Without the enzyme necessary to process phenylalanine, a dangerous buildup can develop when a person with PKU eats foods that contain protein or eats aspartame, an artificial sweetener. This can eventually lead to serious health problems.

Hope it works♥️✌️

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