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phenylketonuria
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What is Phenylketonuria PKU?
phenylketonuria
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
Is phenylketonuria chromosmal?
peeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee
What is the abbreviation for phenylketonuria?
PKU
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.
What limitations do a person have if they have phenylketonuria?
your mother
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.
Phenylketonuria results from an inability to metabolize?
Phenylalanine.
What type of autosomal disease is phenylketonuria?
recessive
What are the amino acids which can't accumulate?
Phenylketonuria
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