phenylacetate/seizures

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Early Dietary Treated Patients With Phenylketonuria Can Achieve Normal Growth and Mental Development.

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Phenylketonuria is rare genetic disease caused by mutation in gene of phenylalanine (Phe) hydroxylase that converts Phenylalanine into tyrosine. The absence of this enzyme leads to elevation and accumulation of Phenylalanine and, increased phenylketones in urine (hence PKU), and also leads to

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