Definition of Phenylketonuria. Meaning of Phenylketonuria. Synonyms of Phenylketonuria

- Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated PKU can lead to...
- is biosynthesized via the shikimate pathway. The genetic disorder phenylketonuria (PKU) is the inability to metabolize phenylalanine because of a lack...
- malaria. Such disorders include cystic fibrosis, sickle cell disease, phenylketonuria and thal****aemia. Hereditary defects in enzymes are generally inherited...
- mutations in its encoding gene, PAH, can lead to the metabolic disorder phenylketonuria. The reaction is thought to proceed through the following steps: formation...
- first described the disease commonly known as Følling's disease or phenylketonuria (PKU). He was born on 23 August 1888 at Kvam, Steinkjer in Trøndelag...
- be screened for phenylketonuria and hypothyroidism, among other congenital disorders. Hypothesis: "The newborns have phenylketonuria and hypothyroidism"...
- development. Medium-chain acyl-coenzyme A dehydrogenase deficiency (MCADD) Phenylketonuria, a disorder where an error in amino acid metabolism can impair brain...
- synthase (PTPS) deficiency. Also, BH4*2HCL is FDA approved for use in phenylketonuria (PKU), along with dietary measures. However, most people with PKU have...
- n-3 long-chain polyunsaturated fatty acid values in patients with phenylketonuria: a systematic review and meta-analysis". Nutrition Research. 33 (7):...
- although in some people, malnutrition may occur. Individuals with phenylketonuria (PKU) must keep their intake of phenylalanine – an essential amino...