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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">ppharm</journal-id><journal-title-group><journal-title xml:lang="ru">Педиатрическая фармакология</journal-title><trans-title-group xml:lang="en"><trans-title>Pediatric pharmacology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1727-5776</issn><issn pub-type="epub">2500-3089</issn><publisher><publisher-name>Издательство «ПедиатрЪ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15690/pf.v11i1.895</article-id><article-id custom-type="elpub" pub-id-type="custom">ppharm-139</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>РЕДКИЕ БОЛЕЗНИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>RARE DISEASES</subject></subj-group></article-categories><title-group><article-title>ПРОПИОНОВАЯ АЦИДУРИЯ У РЕБЕНКА В ВОЗРАСТЕ 5 МЕСЯЦЕВ</article-title><trans-title-group xml:lang="en"><trans-title>PROPIONIC ACIDURIA IN A 5-MONTH-OLD CHILD</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>Фоминых</surname><given-names>Л. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Fominykh</surname><given-names>L. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук, ассистент кафедры педиатрии Института последипломного образования Кировской государственной медицинской академии</p></bio><bio xml:lang="en"><p>MD, assistant at the department of pediatrics of the Institute of postgraduate education of Kirov State Medical Academy</p></bio><email xlink:type="simple">dob.fominykh@yandex.ru</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>Соловьева</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Solovyeva</surname><given-names>G. V.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вязникова</surname><given-names>М. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Vyaznikova</surname><given-names>M. L.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Муратова</surname><given-names>Н. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Muratova</surname><given-names>N. G.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Серебреникова</surname><given-names>Т. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Serebrenikova</surname><given-names>T. E.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Костючек</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kostyuchek</surname><given-names>E. A.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Институт последипломного образования Кировской государственной медицинской академии<country>Россия</country></aff><aff xml:lang="en">Institute of Postgraduate Education of the Kirov State Medical Academy<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Институт последипломного образования Кировской государственной медицинской академии, &#13;
Российская Федерация<country>Россия</country></aff><aff xml:lang="en">Institute of Postgraduate Education of the Kirov State Medical Academy, Russian Federation<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">Детская областная клиническая больница, Киров, Российская Федерация<country>Россия</country></aff><aff xml:lang="en">Children’s Regional Clinical Hospital, Kirov, Russian Federation<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>15</day><month>02</month><year>2014</year></pub-date><volume>11</volume><issue>1</issue><issue-title>Педиатрическая фармакология</issue-title><fpage>52</fpage><lpage>54</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Фоминых Л.Д., Соловьева Г.В., Вязникова М.Л., Муратова Н.Г., Серебреникова Т.Е., Костючек Е.А., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Фоминых Л.Д., Соловьева Г.В., Вязникова М.Л., Муратова Н.Г., Серебреникова Т.Е., Костючек Е.А.</copyright-holder><copyright-holder xml:lang="en">Fominykh L.D., Solovyeva G.V., Vyaznikova M.L., Muratova N.G., Serebrenikova T.E., Kostyuchek E.A.</copyright-holder><license 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.pedpharma.ru/jour/article/view/139">https://www.pedpharma.ru/jour/article/view/139</self-uri><abstract/><trans-abstract xml:lang="en"><p>Propionic aciduria is a rare hereditary metabolic disease with autosomal-recessive inheritance mode associated with organic acid metabolic disorder. Early diagnostics is difficult as clinical symptoms caused by metabolic defects are often observed at hypoxicischemic central nervous system lesion, brain malformations and intrauterine infections. Laboratory examination reveals increased concentration of organic acids in blood and urine. The article presents observation of propionic aciduria in a 5-month-old child.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>наследственные болезни обмена веществ</kwd><kwd>пропионовая ацидурия</kwd><kwd>дети</kwd><kwd>диагностика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hereditary metabolic diseases</kwd><kwd>propionic aciduria</kwd><kwd>children</kwd><kwd>diagnostics</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">Scriver C. R., Beaudet A. L., Sly W. S. The Metabolic and Molecluar Bases of Inherited Diseases. 8th end. New York: McGraw-Hill. 2001. 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