IDENTIFICATION OF CONCOMITANT PATHOLOGY AND ANALYSIS OF TREATMENT IN CHILDREN WITH CLEFT LIP AND PALATE

Authors

  • Mirzaeva F.A. Asia International University

DOI:

https://doi.org/10.55640/

Keywords:

congenital cleft lip and palate, congenital anomalies, lifestyle, risk factors, medical care.

Abstract

Solving the problems of treating children with congenital cleft lip and palate is the most urgent task of maxillofacial surgery. Along with the high birth rate of children with this pathology, it also causes severe morphological and functional disorders in the body of newborns. Early transition to artificial nutrition due to the impossibility of breastfeeding reduces the body's resistance, which leads to a delay in the growth and development of the child. Children with this pathology from the first months are significantly different from their peers. According to the literature data, it is known that congenital cleft lip and palate are often combined with anomalies in the development of other organs, which ranges from 4 to 9.8%. But  according to the results of a study in our republic, these figures can be doubled.[.Yoshiev A.M., Davydova A.K. 2013].

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References

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Published

2026-02-25

Issue

Vol. 5 No. 02 (2026): Journal of Multidisciplinary Sciences and Innovations

Section

Articles

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Authors retain the copyright of their manuscripts, and all Open Access articles are disseminated under the terms of the Creative Commons Attribution License 4.0 (CC-BY), which licenses unrestricted use, distribution, and reproduction in any medium, provided that the original work is appropriately cited. The use of general descriptive names, trade names, trademarks, and so forth in this publication, even if not specifically identified, does not imply that these names are not protected by the relevant laws and regulations.

How to Cite

IDENTIFICATION OF CONCOMITANT PATHOLOGY AND ANALYSIS OF TREATMENT IN CHILDREN WITH CLEFT LIP AND PALATE. (2026). Journal of Multidisciplinary Sciences and Innovations, 5(02), 2235-2237. https://doi.org/10.55640/

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