PKU has various meanings in the Fda category. Discover the full forms, definitions, and usage contexts of PKU in Fda.
A human disease caused by a genetic deficiency in the enzyme that converts phenylalanine to tyrosineThe immediate cause of the disease is an excess of phenylalanine, which can be alleviated by a diet low in phenylalanine. A disease caused by the inability to convert phenylalanine into tyrosine, which results in excess phenylalanine and its secondary metabolites; the disease is characterized by severe retardation.
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