FREQUENCY AND CLINICAL VARIANTS OF BILIARY TRACT IN CHILDREN

At the same time, the proportion of cholelithiasis in children with an upward trend is increasing. In the structure of the pathology of the biliary tract, there is a significant increase in both dysfunctional disorders and diseases of an metabolic-inflammatory nature (1). A certain role in the formation of the pathology of the biliary tract is played by congenital anomalies of the gallbladder and biliary tract. The studies carried out indicate the frequency of lesions of the biliary tract in school-age children. Comparative analysis of the data obtained in a comprehensive study allows differentiating the pathology of the biliary tract, but with a clinical manifestation, and also confirms the informative value of X-ray and ultrasound studies to clarify the diagnosis

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-08
DOI
https://doi.org/10.5281/zenodo.14992150
Primary Topic
Chromosomal and Genetic Variations
Type
article
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article

FREQUENCY AND CLINICAL VARIANTS OF BILIARY TRACT IN CHILDREN

Zenodo (CERN European Organization for Nuclear Research)
Chromosomal and Genetic Variations
article

FREQUENCY AND CLINICAL VARIANTS OF BILIARY TRACT IN CHILDREN

article en

Abstract

At the same time, the proportion of cholelithiasis in children with an upward trend is increasing. In the structure of the pathology of the biliary tract, there is a significant increase in both dysfunctional disorders and diseases of an metabolic-inflammatory nature (1). A certain role in the formation of the pathology of the biliary tract is played by congenital anomalies of the gallbladder and biliary tract. The studies carried out indicate the frequency of lesions of the biliary tract in school-age children. Comparative analysis of the data obtained in a comprehensive study allows differentiating the pathology of the biliary tract, but with a clinical manifestation, and also confirms the informative value of X-ray and ultrasound studies to clarify the diagnosis

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 67%
Chromosomal and Genetic Variations
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