WebPhenylketonuria (PKU) is a genetic condition that causes elevated levels of a substance called phenylalanine to build up in your body. Phenylalanine is found in the body as part of … WebDeveloped for patients with phenylketonuria (PKU) and their parents to cover the physical, emotional, and social impacts of PKU and its treatment on patients’ lives Therapeutic area Congenital, Hereditary, and Neonatal Diseases and Abnormalities Nutritional and Metabolic Diseases Rare disease (Orphanet definition) Therapeutic indications
The impact on quality of life of diet restrictions and ... - Springer
WebDeveloped for patients with phenylketonuria (PKU) and their parents to cover the physical, emotional, and social impacts of PKU and its treatment on patients’ lives Therapeutic area … Webirreversible brain damage and intellectual disabilities within the first few months of life behavioral problems and seizures in older children A less severe form of PKU is called … bandcamp sample packs
Measuring Burden of Illness in Phenylketonuria (PKU ... - PubMed
Webreported that phenylketonuria affects a range of neuropsychological speed tests, with higher phenylalanine concentrations associated with a more pronounced deficit; responses in children to a choice reaction time test … Web18. jan 2024 · Phenylketonuria (PKU) is an autosomal recessive inherited disorder characterised by a deficiency in phenylalanine hydroxylase. Untreated, PKU is associated with a wide range of cognitive and psychiatric sequelae. Web29. nov 2024 · Phenylketonuria (PKU) is a metabolic disorder leading to a deficiency in the metabolism of phenylalanine (Phe). Elevated Phe levels in the blood, tissue and brain may lead to emotional, cognitive, and physical symptoms in adults. To control blood Phe levels, most individuals with PKU need to follow a strict, life-long Phe-restricted diet. bandcamp saver