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University of Groningen Phenylketonuria Mazzola, Priscila...Phenylketonuria (PKU, MIM 261600) is an autosomal recessive disease characterized by high levels of phenylalanine (Phe)
Phenylketonuria (PKU). PKU at a Glance b Name of disorder: Phenylketonuria (PKU) b OMIM number: 261600 b inheritance pattern: autosomal recessive.
A Genetic Defect in Amino Acid Metabolism: Phenylketonuria ...
Phenylketonuria: An Inborn Error of Phenylalanine Metabolism...Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism resulting from deficiency
Phenylketonuria (PKU) - Complex Carbohydrate Research
5.01.585 Pharmacologic Treatment of PhenylketonuriaOct 01, 2019 · Phenylketonuria (PKU) is a rare, genetic disease that is typically screened for at birth. Children with untreated
The PKU diet at school...A practical guide for schools catering for a child with phenylketonuria (PKU) The PKU diet at school 2 All children regardless of their ethnicity, religion
Phe´nylce´tonurie progressant a` l’aˆge adulte ... · 1. Introduction Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the hepatic