What Causes Phenylketonuria?CausesP

What Causes Phenylketonuria?
Causes
PKU is an inherited condition caused by a defect in the PAH gene. The PAH gene helps create phenylalanine hydroxylase, the enzyme responsible for breaking down phenylalanine. A dangerous buildup of phenylalanine can occur when someone eats high-protein foods, such as eggs and meat. Both parents must pass on a defective version of the PAH gene for their child to inherit the disorder. If just one parent passes on an altered gene, the child won’t have any symptoms, but they’ll be a carrier of the gene.

Results (Indonesian) 1:

Apa penyebab Fenilketonuria?PenyebabPKU adalah kondisi warisan yang disebabkan oleh Cacat gen PAH. Gen PAH membantu menciptakan fenilalanin enzim, enzim yang bertanggung jawab untuk mendobrak fenilalanin. Penumpukan berbahaya fenilalanin dapat terjadi ketika seseorang makan makanan protein tinggi, seperti telur dan daging. Kedua orang tua harus lulus pada versi Cacat gen PAH anak mereka mewarisi gangguan. Jika hanya satu orangtua melewati gen berubah, anak tidak memiliki gejala, tetapi mereka akan menjadi pembawa gen.