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A PKU test is for determining if a newborn has an amino acid that breaks down a common food/drink ingredient called phenylalanine. Without this amino acid a person can have brain dysfunction or even die if they ingest this substance. Therefore it is tested for in newborns. Even if the person is missing the PK enzyme the person can still lead a normal life by avoiding things that contain phenylalanin.
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∙ 14y ago
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What is phenylketonuria?
phenylketonuria
What is Phenylketonuria PKU?
phenylketonuria
Why do they do a phenylketonuria test?
Because if it is left untreated it can cause brain damage and severe mental retardation
What is the basic chemistry involved in the FeCl3 test for phenylketonuria?
fecl3 reacts with the -OH group which gives the purple colur
What is the genetic disorder characterized by a missing digestive enzyme?
Phenylketonuria
What percentage of the world's population has phenylketonuria?
2.42% of the world's population has Phenylketonuria (pku)
What is the abbreviation for phenylketonuria?
PKU
Is phenylketonuria chromosmal?
peeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee
Why do you think a baby is not tested for phenylketonuria immediately after it is born?
A test for phenylketonuria (PKU) is commonly done in a lot of countries. It's included in the baby's newborn screening panel. About the only reason for not testing for PKU is lack of resources of those providing care in the country, community or at the location of the baby's birth.
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.
