Food Regime for Phenylketonuria: Presenting Complications and Possible Solutions
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DOI: 10.2147/jmdh.s330845
Abstract: Abstract In the category of rare inherited genetic disorders, phenylketonuria is a prominent example. Here, the defective phenylalanine hydroxylase enzyme fails to catalyze conversion of phenylalanine to tyrosine. This leads to not only excess deposition… read more here.
Keywords: possible solutions; food; food regime; phenylketonuria presenting ... See more keywords