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phenylketonuria
/,fɛnəl,kit'ənʊriə/
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phenylketonuria
noun
a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency
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pku
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type of:
inborn error of metabolism
Definition that contains phenylketonuria
pku test
a test of newborn infants for phenylketonuria
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