ISJ Theoretical & Applied Science 09(101) 2021

Philadelphia, USA

Ibragimov, D. D., Mavlyanova, U. M., Gaffarov, U. B., Kuchkorov, F. Sh., & Akramov, H. M.

The case of hemifacial microsomy in blood brothers.

Full Article: PDF

Scientific Object Identifier: http://s-o-i.org/1.1/TAS-09-101-115

DOI: https://dx.doi.org/10.15863/TAS.2021.09.101.115

Language: English

Citation: Ibragimov, D. D., Mavlyanova, U. M., Gaffarov, U. B., Kuchkorov, F. Sh., & Akramov, H. M. (2021). The case of hemifacial microsomy in blood brothers. ISJ Theoretical & Applied Science, 09 (101), 793-795. Soi: http://s-o-i.org/1.1/TAS-09-101-115 Doi: https://dx.doi.org/10.15863/TAS.2021.09.101.115

Pages: 793-795

Published: 30.09.2021

Abstract: The aim of this work was to present a clinical observation of a case of hemifacial microsomia in blood brothers who applied to maxillofacial surgery. Patient S. 31 years old. He entered the department of maxillofacial surgery of the city medical association of Samarkand with the aim of obtaining a medical opinion about VTEK. Goldenhar syndrome (oculoauriculo-vertebral dysplasia, hemifacial microsomia, disease of the oculoauriculo-vertebral spectrum) is a rare congenital disease associated with damage to structures emanating from the first and second branchial arches. A clinical example indicates the need for a comprehensive examination and a thorough collection of anamnesis of the disease of patients with Goldenhar syndrome for the timely implementation of appropriate treatment and rehabilitation measures and improving the quality of life of children.

Key words: Goldenhar syndrome, atresia of the external auditory canal, hypoplasia of facial muscles.