prior to birth, the mother's enzyme level prevents accumulation of the chemical
prior to birth, the mother's enzyme level prevents accumulation of the dangerous chemical
until they die
Infants are tested for PKU when they are first born. Brain damage occurs within days of birth, if PKU is not diagnosed and treated. Phenylketonuria is not found in adults, only newborn infants.
Because of it's rarity. In the world 1 out of 25 000 is affected by PKU. In the States, 1 out of 15 000 is affected, Turkey 1 out of 2 300. In Finland, however, only one out of 100 000 has PKU. When the chances for the child are 0,00001% to have PKU, it's not routinely tested on all infants. 20 out of 34 hospitals test for PKU, but most only if both parents are foreign and only three hospital test if one of the parent is foreign. None of them test PKU on every child.
until they die
Phenylketonuria (PKU) occurs in approximately 1 in 10,000 to 15,000 newborns in the United States. Screening programs help to detect PKU early so that affected individuals can receive treatment to prevent complications.
PKU is an autosomal recessive genetic disorder, meaning it is not influenced by the sex chromosomes. Both males and females can be affected by PKU if they inherit two copies of the mutated gene.
Phenylketonuria (PKU) is not an eating disorder. It is an inherited disorder which the body cannot break down phenylalanine, which is a part of protein. If PKU is not treated soon after birth, it can cause brain and nervous system damage.
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.
PKU, can cause a serious metal retardess, and a (specific protein).
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.