RESUMO

The expression and activity of phenylalanine hydroxylase was studied in the liver of a fetus aborted after prenatal diagnosis of phenylketonuria. No phenylalanine hydroxylase enzymatic activity or immunoreactive protein was detectable in the PKU liver specimen, though both enzymatic activity and immunoreactive protein were detectable in control specimens of similar gestational age. Phenylalanine hydroxylase messenger RNA of normal size was present in the PKU fetal liver at normal abundance. These results confirm the genetic diagnosis of PKU in this fetus and indicate that the mutations in this fetus affect translation or stability of the phenylalanine hydroxylase protein.

Assuntos

Fígado/enzimologia , Fenilalanina Hidroxilase/metabolismo , Fenilcetonúrias/enzimologia , Aborto Induzido , Feminino , Feto/enzimologia , Humanos , Recém-Nascido , Fígado/embriologia , Fenilalanina Hidroxilase/genética , Fenilcetonúrias/diagnóstico , Fenilcetonúrias/genética , Polimorfismo de Fragmento de Restrição , Gravidez , Diagnóstico Pré-Natal