Metadata
Author: ParaCrawl Corpus
Data
English[en]
This is a non-hereditary disease, which principal possible causes are either the immaturity or deficiency of p-hydroxiphenylpiruvate oxidase hepatic enzyme, produced by variations in its perinatal formation, a high phenylalanine or tyrosine consumption or an ascorbic acid deficiency.
Spanish[es]
No es hereditaria y dentro de las posibles causas se encuentran: una deficiencia o inmadurez de la enzima p-hidroxifenilpiruvato oxidasa hepática producto a variaciones en su formación en el periodo perinatal, consumo elevado de fenilalanina o tirosina y por deficiencia de ácido ascórbico.