Medical dictionary. 2011.
hyperphenylalaninemia — The presence of abnormally high blood levels of phenylalanine, which may or may not be associated with elevated tyrosine levels, in newborn infants (premature and full term), associated with the heterozygous state of phenylketonuria, maternal… … Medical dictionary
atypical phenylketonuria — non PKU hyperphenylalaninemia; the term was formerly used to denote tetrahydrobiopterin deficiency disorders … Medical dictionary
variant phenylketonuria — a third category sometimes used in classification of hyperphenylalaninemia due to defects in phenylalanine hydroxylase; it comprises individuals with phenylalanine tolerance intermediate between those with phenylketonuria and those with non PKU… … Medical dictionary
Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 … Wikipedia
Dominance (genetics) — For other uses, see Dominance. A pedigree chart shows how genes are inherited. Dominance in genetics is a relationship between two variant forms (alleles) of a single gene, in which one allele masks the effect of the other in influencing some… … Wikipedia
Phenylalanine — Phe redirects here. For other uses, see Phe (disambiguation). Phenylalanine … Wikipedia
Tetrahydrobiopterin — Systematic (IUPAC) name (6R) 2 Amino 6 [(1R,2S) 1,2 dihydroxypropyl] 5,6,7,8 tetrahydropteridin 4(1H) one Clinical data … Wikipedia
Phenylalanine hydroxylase — predicted 3D structure of phenylalanine hydroxylase … Wikipedia
Phénylcétonurie — Classification et ressources externes CIM 10 E70.0 CIM 9 270.1 OMIM … Wikipédia en Français
Newborn screening — See also: Apgar score Newborn screening Intervention MeSH D015997 Newborn screening is the process by which infants are screened shortly after birth for a list of disorders that are treatable, but di … Wikipedia
