You will have had a blood test that would have diagnosed that shortly after your birth. If you want to test that, go eat a couple packs of Equal sweetener...if you get deathly ill, you probably have PKU.
phenylketonuria
phenylketonuria
Because if it is left untreated it can cause brain damage and severe mental retardation
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.
2.42% of the world's population has Phenylketonuria (pku)
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.
peeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee
PKU
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.
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.