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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Kazan medical journal</journal-id><journal-title-group><journal-title xml:lang="en">Kazan medical journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Казанский медицинский журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0368-4814</issn><issn publication-format="electronic">2587-9359</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">101707</article-id><article-id pub-id-type="doi">10.17816/kazmj101707</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">A case of Markiafava-Mikeli disease</article-title><trans-title-group xml:lang="ru"><trans-title>Случай болезни Маркиафава-Микели</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Korolev</surname><given-names>A. M.</given-names></name><name xml:lang="ru"><surname>Королев</surname><given-names>А. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>info@eco-vector.com</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Kirov Regional Hospital</institution></aff><aff><institution xml:lang="ru">Больница Кировского облздрава</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="1957-12-15" publication-format="electronic"><day>15</day><month>12</month><year>1957</year></pub-date><volume>38</volume><issue>2-3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>105</fpage><lpage>107</lpage><history><date date-type="received" iso-8601-date="2022-02-25"><day>25</day><month>02</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-02-25"><day>25</day><month>02</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 1957, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 1957, Эко-Вектор</copyright-statement><copyright-year>1957</copyright-year><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://kazanmedjournal.ru/kazanmedj/article/view/101707">https://kazanmedjournal.ru/kazanmedj/article/view/101707</self-uri><abstract xml:lang="en"><p>Chronic hemolytic anemia with intravascular hemolysis, Markiafau-Mikeli disease, first described in 1911, is an extremely rare disease. According to Grosby, only 162 cases have been described in the world literature. But, as G.V. Osechenskaya rightly points out, despite the rarity of the disease, the severity of the course of the disease, difficulty of diagnosis, lack of reliable means of treatment make every case to be carefully studied. This prompts us to publish our observation.</p></abstract><trans-abstract xml:lang="ru"><p>Хроническая гемолитическая анемия с внутрисосудистым гемолизом— болезнь Маркиафава-Микели, описанная впервые в 1911 году,— чрезвычайно редкое заболевание. По данным Гросби, в мировой литературе описано всего 162 случая. Но, как справедливо указывает Г. В. Осеченская, несмотря на редкость заболевания, тяжесть течения болезни, трудность диагностики, отсутствие надежных средств лечения заставляют тщательно изучать каждый случай. Это побуждает опубликовать наше наблюдение.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Kazan Medical archive</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>Казанский медицинский архив</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>П. М. Альперин и М. Я. Аншевиц. Терапевтический архив, 1940, том 18, вып. 5, стр. 502—516.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Ф. М. Василевская. Клиническая медицина, 1941, том 19, № 4, стр. 43—56.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>X. X. Владос, Г. В. Осеченская и А. П. Белоусов. Терапевтический архив, том 24, вып. 3, стр. 44—50.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>W. H. Grоsbу, Blood, 1953, 8, № 9, р. 769—812 (цитировано по Г. В. Осеченской).</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>И. А. Кассирский, Г. А. Алексеев. Клиническая гематология, Медгиз. 1955, стр. 232—235.</mixed-citation></ref></ref-list></back></article>
