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.
your mother
phenylketonuria
normal as any other person normal as any other person
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 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.
2.42% of the world's population has Phenylketonuria (pku)
Phenylketonuria
PKU
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Phenylketonuria is a genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.