Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a - Hyperphenylalanemia - Document - PDFSEARCH.IO

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	Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a Add to Reading List Document Date: 2011-11-10 05:39:05 Open Document File Size: 22,36 KB Share Result on Facebook MedicalCondition Phenylketonuria (PKU) Phenylketonuria / inherited autosomal recessive disorder / deficiency / mental retardation / PKU / seizures / / / Position Metabolic Specialist / / ProvinceOrState Maine / / SocialTag Medicine Biology Pediatrics PKU Phenylalanine Newborn screening Dominance Tetrahydrobiopterin deficiency Hyperphenylalanemia Health

Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the aAdd to Reading List