“MORPHOLOGICAL AND MORPHOMETRIC ANALYSIS OF CYSTIC FIBROSIS IN CHILDREN IN UZBEKISTAN.”

Authors

  • Karataeva Lola Abdullaevna Department of “Physiology and Pathology” of Tashkent State Medical University, Tashkent, Uzbekistan Author
  • Rakhmonova Shakhnoz Kakhhorovna Department of “Physiology and Pathology” of Tashkent State Medical University, Tashkent, Uzbekistan. Author

Keywords:

cystic fibrosis, intestinal form, immunohistochemistry

Abstract

Cystic fibrosis or cystic fibrosis or Landsteiner-Fanconi disease is a hereditary systemic autosomal recessive exocrinopathy, characterized by early clinical manifestations of the respiratory tract, gastrointestinal system and other organs. Among all the diseases that occur in newborns, cystic fibrosis occurs in 1 in 2 thousand children

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Published

2025-12-21

Issue

Vol. 3 No. 12 (2025): WEJMMS

Section

Articles

License

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

How to Cite

“MORPHOLOGICAL AND MORPHOMETRIC ANALYSIS OF CYSTIC FIBROSIS IN CHILDREN IN UZBEKISTAN.”. (2025). Western European Journal of Medicine and Medical Science, 3(12), 83-86. https://westerneuropeanstudies.com/index.php/3/article/view/3133