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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
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Document Date: 2011-11-10 05:39:05
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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