Analysis of signs and symptoms in patients with craniofacial microsomia and their treatment

Relevance . Craniofacial microsomia is a collective definition combining congenital pathologies of organs developing from the first and second branchial arches. However, affiliation various to this disease remains controversial. For reason, there are no standardized indications for timing methods treatment. Materials This paper analyzes results examinations conducted 2011 2021in 89 children adolescents 1 18 years with craniofacial microsomia. Results Patient groups were allocated according pathology severity their age, offered vari- ous treatments depending on phenotype variant. Conclusions Based international our experience considering anatomical functional changes in microsomia, creating scheme customized multidisciplinary algorithm treat these patients becomes relevant.