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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">vsp</journal-id><journal-title-group><journal-title xml:lang="ru">Вопросы современной педиатрии</journal-title><trans-title-group xml:lang="en"><trans-title>Current Pediatrics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-5527</issn><issn pub-type="epub">1682-5535</issn><publisher><publisher-name>Издательство «ПедиатрЪ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15690/vsp.v19i1.2084</article-id><article-id custom-type="elpub" pub-id-type="custom">vsp-2305</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>КЛИНИЧЕСКОЕ НАБЛЮДЕНИЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL OBSERVATIONS</subject></subj-group></article-categories><title-group><article-title>Клинический случай редкого варианта наследственного дерматоза: энтеропатический акродерматит</article-title><trans-title-group xml:lang="en"><trans-title>Clinical Case of Rare Variant of Inherited Dermatosis: Acrodermatitis Enteropathica</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6940-1588</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хорошева</surname><given-names>Е. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Khorosheva</surname><given-names>Elena Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Хорошева Елена Юрьевна - кандидат медицинских наук, доцент кафедры детских болезней педиатрического факультета Тюменского ГМУ.</p><p>625023, Тюмень, ул. Одесская, д. 54А.</p><p>Тел.: +7 (3452) 28-74-70</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><email xlink:type="simple">dr.khorosheva@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2014-4709</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузьмичева</surname><given-names>К. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuzmicheva</surname><given-names>Kseniya P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюмень.</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8968-3925</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Храмова</surname><given-names>Е. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Khramova</surname><given-names>Elena B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюмень.</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2566-5370</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рычкова</surname><given-names>О. A.</given-names></name><name name-style="western" xml:lang="en"><surname>Rychkova</surname><given-names>Olga A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюмень.</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8955-2052</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Горохова</surname><given-names>Н. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Gorokhova</surname><given-names>Natalya E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюмень.</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9987-4899</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Малинина</surname><given-names>E. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Malinina</surname><given-names>Elena I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тюмень.</p></bio><bio xml:lang="en"><p>Tyumen.</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Тюменский государственный медицинский университет; Областная клиническая больница № 1</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tyumen State Medical University; Regional Clinical Hospital № 1</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Тюменский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tyumen State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Областная клиническая больница № 1</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Regional Clinical Hospital № 1</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>18</day><month>04</month><year>2020</year></pub-date><volume>19</volume><issue>1</issue><fpage>40</fpage><lpage>45</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Хорошева Е.Ю., Кузьмичева К.П., Храмова Е.Б., Рычкова О.A., Горохова Н.Е., Малинина E.И., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Хорошева Е.Ю., Кузьмичева К.П., Храмова Е.Б., Рычкова О.A., Горохова Н.Е., Малинина E.И.</copyright-holder><copyright-holder xml:lang="en">Khorosheva E.Y., Kuzmicheva K.P., Khramova E.B., Rychkova O.A., Gorokhova N.E., Malinina E.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://vsp.spr-journal.ru/jour/article/view/2305">https://vsp.spr-journal.ru/jour/article/view/2305</self-uri><abstract><p>Обоснование. Энтеропатический акродерматит является редкой формой наследственных дерматозов. Дебют заболевания у детей ассоциирован с прекращением грудного вскармливания и началом использования продуктов на основе коровьего молока, что затрудняет дифференциальную диагностику акродерматита и аллергодерматозов. Настороженность специалистов в отношении цинкдефицитных состояний при периорифициальном дерматите в соче­тании с алопецией и диареей у детей раннего возраста позволит своевременно установить верный диагноз и опре­делить тактику терапии. Описание клинического случая. В статье представлено описание клинического случая эрозивно-десквамативного акродерматита в сочетании с алопецией и сниженной концентрацией цинка в сыворотке крови. Показана положительная динамика поражения кожи при назначении терапии препаратом сульфата цинка. Заключение. Наличие периорифициального дерматита у ребенка любого возраста требует исключения цинкдефицитных состояний.</p></abstract><trans-abstract xml:lang="en"><p>Background. Acrodermatitis enteropathica is the rare form of inherited dermatoses. The disease onset in children is associated with the ablactation and the beginning of cow milk products use, that makes differential diagnosis of acrodermatitis and allergic dermatoses pretty difficult. The caution of specialists to hypozincemia at periorificial dermatitis combined with alopecia and diarrhea in infants will allow to establish correct diagnosis and choose management timely. Clinical Case Description. The clinical case of erosive- desquamative dermatitis combined with alopecia and hypozincemia is presented in this article. Positive dynamics of skin lesion due to administration with zinc sulfate medication is shown. Conclusion. The presence of periorificial dermatitis in the child of any age requires to perform the differential diagnosis for zinc deficiency conditions.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>дети</kwd><kwd>клинический случай</kwd><kwd>дефицит цинка</kwd><kwd>энтеропатический акродерматит</kwd><kwd>эрозивно-десквамативный дерматит</kwd><kwd>периорифициальный дерматит</kwd><kwd>эрозии</kwd><kwd>сульфат цинка</kwd></kwd-group><kwd-group xml:lang="en"><kwd>children</kwd><kwd>clinical case</kwd><kwd>hypozincemia</kwd><kwd>acrodermatitis enteropathica</kwd><kwd>erosive-desquamative dermatitis</kwd><kwd>periorificial dermatitis</kwd><kwd>erosions</kwd><kwd>zinc sulfate</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Не указан.</funding-statement><funding-statement xml:lang="en">Not specified.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Mortz CG, Brockow K, Bindslev-Jensen C, Broesby-Olsen S. 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