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phenylketonuria
Tito Nolan
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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
What is the abbreviation for phenylketonuria?
PKU
Is phenylketonuria chromosmal?
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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.
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
Are there different forms of PKU or phenylketonuria?
No.
What limitations do a person have if they have phenylketonuria?
your mother
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 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.
What are the amino acids which can't accumulate?
Phenylketonuria
