(PKU) PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria, or PKU, is an autosomal recessive defect in phenylalanine metabolism caused by the absence of the liver enzyme phenylalanine hydroxylase. Infants with - Phenylalanine hydroxylase - Document - PDFSEARCH.IO

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	(PKU) PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria, or PKU, is an autosomal recessive defect in phenylalanine metabolism caused by the absence of the liver enzyme phenylalanine hydroxylase. Infants with Add to Reading List Document Date: 2007-06-25 16:37:39 Open Document File Size: 75,88 KB Share Result on Facebook MedicalCondition microcephaly / PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria / vomiting / mental retardation / disorder / PKU / seizures / autosomal recessive metabolic disorder / Allied Disorders / classic phenylketonuria / Reference Phenylketonuria / eczema / / MedicalTreatment Total parenteral nutrition / / Organization www.web.ukonline.co.uk/nspku/healthvisitor.htm National Coalition for PKU / / / Position phenylalanine attending physician / Pediatric Metabolic Specialist / / TVShow A Place of our Own / / URL www.pku-allieddisorders.org / www.web.ukonline.co.uk/nspku/healthvisitor.htm / www.peds.umn.edu/pku / www.listserv.emory.edu/archives/pku-support-l.html / www.tylerforlife.com/index.html / www.pkudamon1978.homestead.com / www.pkunetwork.org / / SocialTag Aromatic amino acids Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Mental retardation Phenylketonuria Phenylalanine PKU Newborn screening Chemistry

(PKU) PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria, or PKU, is an autosomal recessive defect in phenylalanine metabolism caused by the absence of the liver enzyme phenylalanine hydroxylase. Infants withAdd to Reading List