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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">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">medgen-1674</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>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Клинический полиморфизм и генетическая гетерогенность наследственных заболеваний сетчатки</article-title><trans-title-group xml:lang="en"><trans-title>Clinical polymorphism and genetic heterogeneity of inherited retinal diseases</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зольникова</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zolnikova</surname><given-names>I. V.</given-names></name></name-alternatives><email xlink:type="simple">innzolnikova@hotmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кадышев</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kadyshev</surname><given-names>V. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Марахонов</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Marakhonov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зинченко</surname><given-names>Р. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Zinchenko</surname><given-names>R. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр глазных болезней им. Гельмгольца» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Helmholtz National Medical Research Center of Eye diseases</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Медико-генетический научный центр имени академика Н.П. Бочкова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Centre for Medical Genetics</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>26</day><month>11</month><year>2020</year></pub-date><volume>19</volume><issue>8</issue><fpage>42</fpage><lpage>43</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Зольникова И.В., Кадышев В.В., Марахонов А.В., Зинченко Р.А., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Зольникова И.В., Кадышев В.В., Марахонов А.В., Зинченко Р.А.</copyright-holder><copyright-holder xml:lang="en">Zolnikova I.V., Kadyshev V.V., Marakhonov A.V., Zinchenko R.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.medgen-journal.ru/jour/article/view/1674">https://www.medgen-journal.ru/jour/article/view/1674</self-uri><abstract><p>Наследственные заболевания сетчатки (НЗС) представляют собой класс офтальмологических болезней, в котором выделяют заболевания с преимущественным поражением палочковой системы и заболевания с преимущественным поражением колбочковой системы, включающие макулярные дистрофии. В представленном сообщении описана структура спектра НЗС в клинически полиморфной выборке на основании данных клинических, инструментальных (оптической когерентной томографии, аутофлюоресценции, электроретинографии) и молекулярно-генетических методов диагностики (NGS, секвенирование по Сэнгеру).</p></abstract><trans-abstract xml:lang="en"><p>Inherited retinal disease (IRD) is a class of ophthalmic disorders in which can be classified into diseases of primarily of rod system and with primarily of cone system, which include macular dystrophies. In the presented report the structure of spectrum of IRD in clinically polymorphic is presented on the base of clinical, molecular-genetics and instrumental (OCТ, autofluorescencе, eletroretinography).</p></trans-abstract><kwd-group xml:lang="ru"><kwd>наследственные заболевания сетчатки</kwd><kwd>генетика</kwd><kwd>офтальмология</kwd><kwd>болезнь Штаргардта</kwd><kwd>пигментный ретинит</kwd><kwd>клинический полиморфизм</kwd><kwd>генетическая гетерогенность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hereditary retinal diseases</kwd><kwd>genetics</kwd><kwd>ophthalmology</kwd><kwd>Stargardt’s disease</kwd><kwd>retinitis pigmentosa</kwd><kwd>clinical polymorphism</kwd><kwd>genetic heterogeneity</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
