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

dc.contributor.author	Karataeva Lola Abdullaevna
dc.contributor.author	Rakhmonova Shakhnoz Kakhhorovna
dc.date.accessioned	2025-12-29T12:46:41Z
dc.date.issued	2025-12-21
dc.description.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
dc.format	application/pdf
dc.identifier.uri	https://westerneuropeanstudies.com/index.php/3/article/view/3133
dc.identifier.uri	https://asianeducationindex.com/handle/123456789/19699
dc.language.iso	eng
dc.publisher	Western European Studies
dc.relation	https://westerneuropeanstudies.com/index.php/3/article/view/3133/2183
dc.rights	https://creativecommons.org/licenses/by-nc/4.0
dc.source	Western European Journal of Medicine and Medical Science; Vol. 3 No. 12 (2025): WEJMMS; 83-86
dc.source	2942-1918
dc.subject	cystic fibrosis
dc.subject	intestinal form
dc.subject	immunohistochemistry
dc.title	“MORPHOLOGICAL AND MORPHOMETRIC ANALYSIS OF CYSTIC FIBROSIS IN CHILDREN IN UZBEKISTAN.”
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.type	Peer-reviewed Article

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