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People with PKU are more likely to have fair skin, light hair, and blue eyes due to the lack of pigment but in general look no different than you, me, or anyone else.

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What limitations do a person have if they have phenylketonuria?

your mother


What is phenylketonuria?

phenylketonuria


What is the life expectancy of a person with phenylketonuria?

normal as any other person normal as any other person


What is Phenylketonuria PKU?

phenylketonuria


What is the treatment for phenylketonuria?

The best treatment of phenylketonuria is a diet that is extremely low in phenylalanine during childhood. A person can also take fish oil supplements and iron supplements to help treat some of the symptoms.


A person who has what is unable to break down the amino acid phenylalanine?

A person with phenylketonuria (PKU) is unable to break down the amino acid phenylalanine due to a deficiency in the enzyme phenylalanine hydroxylase. This can lead to a build-up of phenylalanine in the body, which can be toxic to the brain and nervous system if not controlled through dietary restrictions.


What percentage of the world's population has phenylketonuria?

2.42% of the world's population has Phenylketonuria (pku)


What is the genetic disorder characterized by a missing digestive enzyme?

Phenylketonuria


What is the abbreviation for phenylketonuria?

PKU


Is phenylketonuria chromosmal?

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How long did it take to discover phenylketonuria?

Phenylketonuria is a genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway


Is phenylketonuria a learning disability?

Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.