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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">clinmed</journal-id><journal-title-group><journal-title xml:lang="ru">Клиническая медицина</journal-title><trans-title-group xml:lang="en"><trans-title>Clinical Medicine (Russian Journal)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0023-2149</issn><issn pub-type="epub">2412-1339</issn><publisher><publisher-name>ООО «Медицинское информационное агентство»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.30629/0023-2149-2024-102-5-6-385-399</article-id><article-id custom-type="elpub" pub-id-type="custom">clinmed-855</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Множественная системная атрофия</article-title><trans-title-group xml:lang="en"><trans-title>Multiple system atrophy</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0632-6653</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Юсупов</surname><given-names>Ф. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Yusupov</surname><given-names>F. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юсупов Фуркат Абдулахатович — д-р мед. наук, профессор, зав. кафедрой неврологии, нерохрургии и психиатрии, медицинского факультета</p><p>Ош</p></bio><bio xml:lang="en"><p>Furkat A. Yusupov — Doctor of Medical Sciences, Professor, Head of the Department of Neurology, Neurosurgery and Psychiatry, Faculty of Medicine</p><p>Osh</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4839-1306</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ыдырысов</surname><given-names>И. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Ydyrysov</surname><given-names>I. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ыдырысов Исматилла Токтосунович — д-р мед. наук, профессор, декан медицинского факультета</p><p>Ош</p></bio><bio xml:lang="en"><p>Ismatilla T. Ydyrysov — Doctor of Medical Sciences, Professor, Dean of the Medical Faculty</p><p>Osh</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4179-9205</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Юлдашев</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Yuldashev</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юлдашев Акмал Акбарович — аспирант кафедры неврологии, нейрохирургии и психиатрии медицинского факультета</p><p>Ош</p></bio><bio xml:lang="en"><p>Akmal A. Yuldashev — postgraduate student of the Department of Neurology, Neurosurgery and Psychiatry of the Medical Faculty</p><p>Osh</p></bio><email xlink:type="simple">akmal.yuldashev.2017@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Ошский государственный университет</institution><country>Кыргызстан</country></aff><aff xml:lang="en"><institution>Osh State University</institution><country>Kyrgyzstan</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>07</day><month>11</month><year>2024</year></pub-date><volume>102</volume><issue>5-6</issue><fpage>385</fpage><lpage>399</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Юсупов Ф.А., Ыдырысов И.Т., Юлдашев А.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Юсупов Ф.А., Ыдырысов И.Т., Юлдашев А.А.</copyright-holder><copyright-holder xml:lang="en">Yusupov F.A., Ydyrysov I.T., Yuldashev A.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.clinmedjournal.com/jour/article/view/855">https://www.clinmedjournal.com/jour/article/view/855</self-uri><abstract><p>Множественная системная атрофия (МСА) — быстро прогрессирующее нейродегенеративное заболевание, характеризующееся наличием вегетативной дисфункции и двигательных нарушений. В большинстве случаев оно возникает у взрослых и проявляется следующими клиническими синдромами различной выраженности: паркинсонизм, мозжечковые нарушения, вегетативная недостаточность, урогенитальная дисфункция и кортикоспинальные нарушения. Трудности диагностики и лечения МСА во многом связаны с неполным пониманием патогенеза заболевания. В этом обзоре обобщаются современные литературные данные об этиологических (в т.ч. генетических) факторах риска, патогенезе, клинике, диагностике, дифференциальной диагностике и лечении множественной системной атрофии.</p></abstract><trans-abstract xml:lang="en"><p>Multiple systemic atrophy (MSA) is a rapidly progressive neurodegenerative disease characterized by the presence of autonomic dysfunction and movement disorders. It occurs in adults in most cases and is manifested by various clinical syndromes with varying degrees of severity, such as parkinsonism, cerebellar dysfunction, autonomic insufficiency, and urogenital and corticospinal dysfunction. Difficulties in diagnosis and treatment are largely due to incomplete understanding of pathogenesis. This review summarizes current literature on etiological, including genetic, risk factors, pathogenesis, clinical presentation, diagnosis, differential diagnosis, and treatment options for MSA.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>множественная системная атрофия</kwd><kwd>нейродегенеративные заболевания</kwd><kwd>паркинсонизм</kwd><kwd>мозжечковые расстройства</kwd></kwd-group><kwd-group xml:lang="en"><kwd>multiple systemic atrophy</kwd><kwd>neurodegenerative diseases</kwd><kwd>parkinsonism</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Fanciulli A., Wenning G.K. Multiple-system atrophy. N. Engl. J. Med. 2015;372(3):249–63. DOI: 10.1056/NEJMra1311488</mixed-citation><mixed-citation xml:lang="en">Fanciulli A., Wenning G.K. Multiple-system atrophy. N. Engl. J. Med. 2015;372(3):249–63. 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