BOLALARDA TUG’MA QIZILO’NGACH ATREZIYALARI

Authors

  • Inoyatova Nazokat Termiz iqtisodiyot va servis universiteti Tibbiyot fakulteti Klinik fanlar kafedrasi
  • Norbek Kholboyev Department of Medicine, Termiz University of Economics and Service, Termiz, Uzbekiston

Keywords:

Congenital esophageal atresia, head tip of the anterior intestine, 4-5 weeks of embryogenesis, inside the cell.

Abstract

Congenital esophageal atresia (TQA) in children is a congenital pathology that occurs as a result of the underdevelopment or loss of some or all parts of the esophagus. Complete or partial loss or obstruction of the esophagus can lead to severe respiratory problems in the child and requires treatment. This article will tell you in detail about congenital esophageal atresia in children and consider its causes, diagnosis, clinical indications and methods of treatment. In esophageal atresia, the upper part of the esophagus ends blindly, while the lower girl often comes into contact with the trachea. It occurs in 5% of cases with chromosomal disorders. The frequency of occurrence in the population is every 1,000, in a 1:1 ratio between males and females, types of esophageal atresia can occur.

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Published

2026-04-21

How to Cite

BOLALARDA TUG’MA QIZILO’NGACH ATREZIYALARI. (2026). INTERNATIONAL CONFERENCE ON MEDICINE, SCIENCE, AND EDUCATION, 3(4), 21-27. https://universalconference.us/universalconference/index.php/icmse/article/view/7043