BOLALARDA FENILKETONURIYA KASALLIGI XAQIDA

Authors

  • Durdona Abduvohidova Alfraganus universiteti Tibbiyot fakulteti davolash ishi yo‘nalishi 24-7 guruh talabasi Author

Keywords:

Phenylketonuria, acids, congenital, Blood, nerve, damage, phenylalanine, newborns, pathology, disease, chronic, course, early disability, patients, treatment, diagnosis, diet, gene.

Abstract

In this article, the treatment of patients with phenylketonuria is continuous and consists of following a strict diet from the moment of diagnosis. The complete elimination of phenylalanine from the diet and the compensation of amino acid deficiency with the help of special dietary supplements allow maintaining normal metabolism in the body. In the article, the causes, consequences, types, treatment methods, physical therapy of the disease; diet for phenylketonuria is given.

Published

2024-10-31

Issue

Vol. 3 No. 10 (2024): Естественные науки в современном мире: теоретические и практические исследования

Section

Articles

How to Cite

BOLALARDA FENILKETONURIYA KASALLIGI XAQIDA. (2024). Natural Sciences in the Modern World, 3(10), 16-19. https://in-academy.uz/index.php/ZDTF/article/view/19928