autosomal recessive genetic disorder characterized by a deficiency in the enzyme phenylalanine hydroxylase Ragnarok (PAH).. Phenylketonuria ID Badges: Identification (PKU) is a rare genetic disorder that results in excessive accumulation of the amino acid, phenylalanine, and reduced levels of the amino. Phenylketonuria
(PKU) can be defined as a rare metabolic disorder caused by a deficiency in the production of the hepatic (liver) enzyme phenylalanine. Genes and Diseases: Phenylketonuria - Brief genetic information. Medline Plus: Phenylketonuria - Definition, 
causes, symptoms and treatment.. Amazon.com: Low Protein Cookery for Books: Virginia E. Schuett by Virginia E. Schuett. Read the latest news and get
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news from over 5000 authoritative medical sources is provided by MedWorm - the RSS. What is the National
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for Phenylketonuria (NSPKU)? The NSPKU exists to help and support people with PKU, their families and carers..
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ASSOCIATIONS ARTICLES HEALTH. ARTICLES. National PKU News and Information HEALTH. Phenylketonuria (PKU) is an inherited block in the breakdown of phenylalanine, a building block
of protein (amino acid). Untreated this results 