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Phenylketonuria as related to Genetics/Birth Defects


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Classical Phenylketonuria; Deficiency Disease, Phenylalanine Hydroxylase; Folling Disease; Phenylalanine Hydroxylase Def... 

 

Phenylketonuria (PKU) is a human genetic disorder that occurs in about 1 in 15,000 births, but the incidence varies widely in different human populations from 1 in 4,500 births among the Irish to fewer than one in 100,000 births among the population of Finland.


Phenylketonuria as related to Genetics/Birth Defects


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November 9, 2009


Page Updated: January 17, 2009
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