Молодежный инновационный вестникМолодежный инновационный вестник2415-7805Федеральное государственное бюджетное образовательное учреждение высшего образования "Воронежский государственный медицинский университет имени Н.Н. Бурденко" Министерства здравоохранения Российской Федерации9968Conference ProceedingsAnanlysis of joint hypermobility syndrome markersKarasevaEkaterinakatya.karaseva.03@bk.ruhttps://orcid.org/0009-0006-6215-9684SesorovaIrinairina-s3@yandex.ruhttps://orcid.org/0000-0001-8993-9927ShnitkovaElenae-shnit@mail.ruhttps://orcid.org/0000-0003-3149-9767Ivanovo State Medical UniversityIvanovi State Medical University2712202413258601504202417062024Copyright © 2024, Karaseva E., Sesorova I., Shnitkova E.2024<p>If diagnosed late, joint hypermobility syndrome can significantly reduce the patients quality of life. The aim of this study was to find significant phenotypic characteristics that could be used in the diagnosis of joint hypermobility syndrome. We have analyzed the frequency of occurrence of phenotypic signs of connective tissue dysplasia in 450 patients with joint hypermobility. It has been shown that joint hypermobility occurs in the population of the Russian Federation with a frequency of 0.29. Among these patients, 61.2% complained of constant or recurrent pain in the spine and/or individual joints. Among patients without arthralgia, 25.4% did not have a sufficient number of markers to diagnose joint hypermobility syndrome. With an increase in the degree of joint hypermobility in patients, the number and frequency of signs of connective tissue dysplasia increases. In the group of patients with moderate and severe joint hypermobility, the following has been recorded: anomalies of the auricle, which are present in 66.6% of respondents; soft and brittle nails (62.8%); scoliosis (55.1%); transverse flatfoot (53%) and malocclusion (60.25%) in people with severe joint hypermobility. Signs with a high frequency of occurrence can be used as minor criteria for the diagnosis of joint hypermobility syndrome, along with the Brighton scale criteria.</p>joint hypermobilityjoint hypermobility syndromeconnective tissue dysplasiaгипермобильность суставовсиндром гипермобильности суставов, дисплазия соединительной ткани1.Всероссийское научное общество кардиологов Наследственные нарушения соединительной ткани. Российские рекомендации. Москва; 2012. -76 с.2.Grahame R. The revised (Brighton 1998) criteria for the diagnosis of benign joint hypermobility syndrome (BJHS) // J. Rheumatol. – 2000.- V. 27. – № 7. P. 1777–9.3.Шниткова Е.В., Савин М.А., Сесорова И.С. Частота встречаемости внешних признаков дизэмбриогенеза у населения российской федерации. Свидетельство о регистрации базы данных RU 2023621444, 11.05.2023. Заявка № 2023621146 от 27.04.2023.4.Сесорова И.С., Шниткова Е.В., Лазоренко Т.В., Марков Д.С. Скрининг-диагностика дисплазии соединительной ткани. Свидетельство о регистрации программы для ЭВМ RU 2017614600, 21.04.2017. Заявка № 2016661349 от 26.10.2016.