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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">transmed</journal-id><journal-title-group><journal-title xml:lang="ru">Трансляционная медицина</journal-title><trans-title-group xml:lang="en"><trans-title>Translational Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-4495</issn><issn pub-type="epub">2410-5155</issn><publisher><publisher-name>Almazov National Medical Research Centre, Saint Petersburg, Russia</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18705/2311-4495-2016-3-2-89-93</article-id><article-id custom-type="elpub" pub-id-type="custom">transmed-182</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>CASE REPORT</subject></subj-group></article-categories><title-group><article-title>СОЧЕТАНИЕ СИНДРОМА НИМАННА-ПИКА (ТИП В) С СОМАТОТРОПНОЙ НЕДОСТАТОЧНОСТЬЮ И ЗАДЕРЖКОЙ СТАРТА ПУБЕРТАТА У ДЕВОЧКИ-ПОДРОСТКА</article-title><trans-title-group xml:lang="en"><trans-title>THE COMBINATION OF NIEMANN-PICK TYPE B SYNDROME WITH GROWTH HORMONE DEFICIENCY AND DELAYED THE START OF PUBERTY</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>Никитина</surname><given-names>Ирина Леоровна</given-names></name><name name-style="western" xml:lang="en"><surname>Nikitina</surname><given-names>Irina L.</given-names></name></name-alternatives><email xlink:type="simple">nikitina0901@gmail.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>Лискина</surname><given-names>Анастасия Сергеевна</given-names></name><name name-style="western" xml:lang="en"><surname>Liskina</surname><given-names>Anastasiya S.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Юхлина</surname><given-names>Юлия Николаевна</given-names></name><name name-style="western" xml:lang="en"><surname>Yuchlina</surname><given-names>Yulia N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Артемьева</surname><given-names>Ирина Юрьевна</given-names></name><name name-style="western" xml:lang="en"><surname>Artemyeva</surname><given-names>Irina Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Федеральное государственное бюджетное учреждение «Северо-Западный Федеральный медицинский исследовательский центр им. В. А. Алмазова» Минздрава России</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>23</day><month>12</month><year>2016</year></pub-date><volume>3</volume><issue>2</issue><fpage>89</fpage><lpage>93</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Никитина И.Л., Лискина А.С., Юхлина Ю.Н., Артемьева И.Ю., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Никитина И.Л., Лискина А.С., Юхлина Ю.Н., Артемьева И.Ю.</copyright-holder><copyright-holder xml:lang="en">Nikitina I.L., Liskina A.S., Yuchlina Y.N., Artemyeva I.Y.</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://transmed.almazovcentre.ru/jour/article/view/182">https://transmed.almazovcentre.ru/jour/article/view/182</self-uri><abstract><p>В статье представлен клинический случай сочетания ранее не описанных эндокринных нарушений: соматотропной недостаточности, задержки полового развития с болезнью Ниманна-Пика (тип В), относящейся к группе лизосомных болезней накопления. Описаны клинические проявления, особенности течения заболевания у данной пациентки, входящие в структуру синдрома Ниманна-Пика (тип В), а также алгоритм дифференциальной диагностики выявленной эндокринной патологии</p></abstract><trans-abstract xml:lang="en"><p>The clinical case of some endocrine disturbances accompanied by Niemann-Pick type B syndrome is presented in this article. There are short stature due to growth hormone deficiency, delay of puberty onset in a girl who was diagnosed with Niemann-Pick type B syndrome that belonging to group of lysosomic diseasescharacterized by severe hepatolienal syndrome. The clinical implications, features of a course of a disease at this patient entering into structure of a syndrome of Niemann-Pick type B, and algorithm of differential diagnosis of the endocrine pathology are described.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>лизосомальные болезни</kwd><kwd>болезнь Ниманна-Пика</kwd><kwd>соматотропная недостаточность</kwd><kwd>задержка пубертата</kwd><kwd>lysosomal disease</kwd><kwd>Niemann-Pick disease</kwd><kwd>growth hormone deficiency</kwd><kwd>delayed puberty</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">Brady RO. The sphingolipidoses. New Eng. J.Med. 1966; 275: 312-318.</mixed-citation><mixed-citation xml:lang="en">Brady RO. The sphingolipidoses. New Eng. J.Med. 1966; 275: 312-318.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Schuchman EH, Levran O, Pireira LV, Desnick RJ. Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SPMD1). Genomics.1992; 12:197-205.</mixed-citation><mixed-citation xml:lang="en">Schuchman EH, Levran O, Pireira LV, Desnick RJ. Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SPMD1). Genomics.1992; 12:197-205.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Dannhausen K, Karlstetter M, Caramoy A, Volz C, Jagle H, Liebisch G et al. Acid sphingomyelinase (aSMase) deficiency leads to abnormal microglia behavior and disturbed retinal function. Biochem Biophys res Commun. 2015; 464(2): 434-40.</mixed-citation><mixed-citation xml:lang="en">Dannhausen K, Karlstetter M, Caramoy A, Volz C, Jagle H, Liebisch G et al. Acid sphingomyelinase (aSMase) deficiency leads to abnormal microglia behavior and disturbed retinal function. Biochem Biophys res Commun. 2015; 464(2): 434-40.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Schuchman EH, Wasserstein MP. Types A and B Niemann-Pick disease. Best Pract Res Clin Endocrinol Me-tab. 2015; 29(2): 237-247.</mixed-citation><mixed-citation xml:lang="en">Schuchman EH, Wasserstein MP. Types A and B Niemann-Pick disease. Best Pract Res Clin Endocrinol Me-tab. 2015; 29(2): 237-247.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Mihno VA, Nikitina IL. Endothelial dysfunction as a risk factor for diabetes and cardiovascular disease. Zabaikalsky medicinsky bulleten=Zabaikalsky medical journal. 2009; 1: 53-64. In Russian. [Михно В.А, Никитина И.Л. Дисфункция эндотелия как фактор риска сахарного диабета и сердечно-сосудистой патологии. Забайкальский медицинский вестник. 2009; 1: 53-64].</mixed-citation><mixed-citation xml:lang="en">Mihno VA, Nikitina IL. Endothelial dysfunction as a risk factor for diabetes and cardiovascular disease. Zabaikalsky medicinsky bulleten=Zabaikalsky medical journal. 2009; 1: 53-64. In Russian. [Михно В.А, Никитина И.Л. Дисфункция эндотелия как фактор риска сахарного диабета и сердечно-сосудистой патологии. Забайкальский медицинский вестник. 2009; 1: 53-64].</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Lloyd-Evans E, Platt FM. Lysosomal Ca(2+) homeostasis: role in pathogenesis of lysosomal storage diseases. Cell Calcium. 2011; 50(2): 200-205.</mixed-citation><mixed-citation xml:lang="en">Lloyd-Evans E, Platt FM. Lysosomal Ca(2+) homeostasis: role in pathogenesis of lysosomal storage diseases. Cell Calcium. 2011; 50(2): 200-205.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Vanier MT. Niemann-Pick disease type C. Orphanet J. Rare Dis. 2010; 5:16.</mixed-citation><mixed-citation xml:lang="en">Vanier MT. Niemann-Pick disease type C. Orphanet J. Rare Dis. 2010; 5:16.</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>
