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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
Will tyrosine test positive in Hopkins-Cole test?
Yes, tyrosine will test positive in the Hopkins-Cole test. This test is used to detect the presence of phenylketonuria (PKU) by identifying the abnormal accumulation of phenylalanine and tyrosine in the blood.
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 basic chemistry involved in the FeCl3 test for phenylketonuria?
The FeCl3 test for phenylketonuria is based on the reaction between phenylpyruvic acid in urine and FeCl3, forming a green-colored complex due to the chelation of the iron ion. This reaction is specific for detecting phenylketonuria because phenylpyruvic acid is elevated in individuals with this disorder, leading to the formation of the colored complex. The color intensity of the complex formed is directly proportional to the concentration of phenylpyruvic acid present in the sample.
Is phenylketonuria chromosmal?
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What is the abbreviation for phenylketonuria?
PKU
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.
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.
