What Phenylketonurics means

Pku is the most serious form of a class of diseases referred to as.This means phenylalanine builds up in the person's blood, urine, and body.Any amino acids that are not needed are broken down further and removed from the body.If pku is not treated, phenylalanine can.Pku is the most serious form of a class of diseases referred to as hyperphenylalaninemia, all of which involve above normal (elevated) levels of phenylalanine in the blood.

Phenylketonuria ( ˌfiːnaɪlˌkiːtəˈnjʊərɪə) n (pathology) a congenital metabolic disorder characterized by the abnormal accumulation of phenylalanine in the body fluids, resulting in various degrees of mental deficiency [c20:Without treatment, children with classic pku develop permanent intellectual disability.As a result, children with pku often will have pale skin, blond hair and blue eyes.Simply put, phenylketonurics means people who suffer from phenylketonuria, whilst phenylalanine is the name of a particular essential amino acid which cannot be made in the human body.Phenylketonurics | definition of phenylketonurics by.

Phenylketonuria (pku) can be defined as a rare metabolic disorder caused by a deficiency in the production of the hepatic (liver) enzyme phenylalanine hydroxylase (pah).Amino acids are the building blocks of protein.Phenylketonuria (pku) is a genetic (inherited) condition in which levels of phenylalanine build up in the blood.There are three forms of phenylalanine:Phenylketonuria (pku) is a rare disorder you inherit from your parents.

The effects of pku can be controlled by a special diet.Reginald garrett and charles grisham in their book, biochemistry.