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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 pub-id-type="doi">10.25557/2073-7998.2022.10.9-11</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-2155</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>КЛИНИЧЕСКИЙ СЛУЧАЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL CASE</subject></subj-group></article-categories><title-group><article-title>Клинический случай наследственного дефицита сахаразы-изомальтазы</article-title><trans-title-group xml:lang="en"><trans-title>Clinical case of congenital Sucrase-isomaltase deficiency</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>Побединская</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Pobedinskaya</surname><given-names>A. I.</given-names></name></name-alternatives><email xlink:type="simple">alena.pobedinskaya74@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГАУЗ Челябинская областная детская клиническая больница</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chelyabinsk Regional Children’s Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>08</day><month>12</month><year>2022</year></pub-date><volume>21</volume><issue>10</issue><fpage>9</fpage><lpage>11</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Побединская А.И., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Побединская А.И.</copyright-holder><copyright-holder xml:lang="en">Pobedinskaya A.I.</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/2155">https://www.medgen-journal.ru/jour/article/view/2155</self-uri><abstract><p>Наследственный дефицит сахаразы-изомальтазы - вид наследственной дисахаридазной непереносимости. Гомозиготные формы данной патологии встречаются c частотой 0,02% в популяции. В статье описан клинический случай этого заболевания, выявленного врачами в Челябинской области. Предоставлены анамнез, клиническая картина, этапы диагностики, а также применяемое лечение.</p></abstract><trans-abstract xml:lang="en"><p>Hereditary sucrase-isomaltase deficiency is a type of hereditary disaccharidase intolerance. Homozygous forms of this pathology occur with a frequency of 0.02% in the population. The article describes a clinical case of this disease, identified by doctors in the Chelyabinsk region. A complete history, stages of the patient’s diagnosis, as well as the treatment used are presented.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>наследственный дефицит сахаразы-изомальтазы</kwd><kwd>дисахаридазная недостаточность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>congenital sucrase-isomaltase deficiency</kwd><kwd>disaccharidase intolerance</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">https://omim.org/entry/222900?search=SI&amp;highlight=si (дата обращения 14.06.2022).</mixed-citation><mixed-citation xml:lang="en">https://omim.org/entry/222900?search=SI&amp;highlight=si (дата обращения 14.06.2022).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">https://allergyfree.ru/category/info/sucrose-izomaltaznaya_failure.html (дата обращения 17.07.2022).</mixed-citation><mixed-citation xml:lang="en">https://allergyfree.ru/category/info/sucrose-izomaltaznaya_failure.html (дата обращения 17.07.2022).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Lloyd M.L., Olsen W.A. A study of the molecular pathology of sucrase-isomaltase deficiency. A defect in the intracellular processing of the enzyme. N Engl J Med. 1987 Feb 19;316(8):438-42. doi: 10.1056/NEJM198702193160804.</mixed-citation><mixed-citation xml:lang="en">Lloyd M.L., Olsen W.A. A study of the molecular pathology of sucrase-isomaltase deficiency. A defect in the intracellular processing of the enzyme. N Engl J Med. 1987 Feb 19;316(8):438-42. doi: 10.1056/NEJM198702193160804.</mixed-citation></citation-alternatives></ref></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>
