No, but you can control it. I think it is a disease that is developmentally dependent with adulthood superseding the disease. In any case, in infants and toddlers one can control the disease by excluding foods containing, or rich in phenylalanine. Google this.
PKU(phenylketonuria)
It's genetic, and recessive - get a test to see if you're a carrier. If you already have it than wait until gene manipulation becomes common.
fecl3 reacts with the -OH group which gives the purple colur
Huntington's disease
Phenylketonuria (PKU) is a condition that makes it impossible to metabolize the amino acid phenylalanine. People with PKU lack an enzyme called phenylalanine hydroxylase, which is required to break down phenylalanine. If left untreated, the buildup of phenylalanine can lead to brain damage and other neurological problems, so individuals with PKU must follow a strict low-phenylalanine diet.
phenylketonuria
phenylketonuria
Persons diagnosed with phenylketonuria must have a specialised diet to prevent further intake of proteins containing the amino acid "phenylanine hydroxylase". If this is not done, and there is no diagnosis, phenylketonuria can lead to severe consequences, one of which is albinism, and ultimately retardation. In other words: EARLY DIAGNOSIS IS IMPORTANT!
2.42% of the world's population has Phenylketonuria (pku)
Phenylketonuria
PKU
peeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.
Phenylketonuria is a genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway
No.
your mother
PKU(phenylketonuria)