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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">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl11814</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-11814</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>Низкорослость и лечение ее гормоном роста</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Dwarfism and its Therapy with Growth Hormone</subject></subj-group></article-categories><title-group><article-title>Клиническая и биохимическая характеристики недостаточности рецепторов к гормону роста (синдром Ларона)</article-title><trans-title-group xml:lang="en"><trans-title>Clinical and biochemical characteristics of growth hormone receptor insufficiency (Larone’s syndrome)</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>Розенблум</surname><given-names>А</given-names></name><name name-style="western" xml:lang="en"><surname>Rosenblom</surname><given-names>A</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.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>Сэвэдж</surname><given-names>М</given-names></name><name name-style="western" xml:lang="en"><surname>Savage</surname><given-names>M</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.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>Блум</surname><given-names>У</given-names></name><name name-style="western" xml:lang="en"><surname>Bloom</surname><given-names>U</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.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>Гевара-Агуирре</surname><given-names>Х</given-names></name><name name-style="western" xml:lang="en"><surname>Gevara-Aguirre</surname><given-names>H</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.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>Розенфелд</surname><given-names>Р</given-names></name><name name-style="western" xml:lang="en"><surname>Rosenfeld</surname><given-names>R</given-names></name></name-alternatives><email xlink:type="simple">probl@endojournals.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>&lt;p&gt;Университет Флориды, США; Больница Св. Варфоломея, Лондон, Великобритания; университетская детская больница, Тюбинген, Германия; Институт эндокринологии, метаболизма и репродукции, Куито, Эквадор; Университет Стэнфорда, США;&lt;/p&gt;</institution><country>Соединённые Штаты Америки</country></aff><aff xml:lang="en"><institution>&lt;p&gt;Florida University, USA; St Bartholomew's Hospital, London, Breat Britain; University children's hospital, Tuebingen, Germany; Endocrinology, metabolism and reproduction institute, Quito, Ecuador; Stanford University, USA&lt;/p&gt;</institution><country>United States</country></aff></aff-alternatives><pub-date pub-type="collection"><year>1994</year></pub-date><pub-date pub-type="epub"><day>15</day><month>04</month><year>1994</year></pub-date><volume>40</volume><issue>2</issue><issue-title>ТОМ 40, №2 (1994)</issue-title><fpage>74</fpage><lpage>77</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Розенблум А., Сэвэдж М., Блум У., Гевара-Агуирре Х., Розенфелд Р., 1994</copyright-statement><copyright-year>1994</copyright-year><copyright-holder xml:lang="ru">Розенблум А., Сэвэдж М., Блум У., Гевара-Агуирре Х., Розенфелд Р.</copyright-holder><copyright-holder xml:lang="en">Rosenblom A., Savage M., Bloom U., Gevara-Aguirre H., Rosenfeld R.</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.probl-endojournals.ru/jour/article/view/11814">https://www.probl-endojournals.ru/jour/article/view/11814</self-uri><abstract><p>Судя по сообщениям, пациенты, число которых превышает 150, с недостаточностью рецептора к гормону роста (НРГР), в основном проживают в Средиземноморском регионе, за исключением 7 больных с индийского субконтинента. В Израиле и Эквадоре отмечаются наибольшие популяционные концентрации больных с НРГР. Для обоих этих мест популяционных концентраций типичным является кровосмешение; также имеются сообщения о подобном явлении в спорадических случаях из других мест. Как при любых наследственных нарушениях, по-видимому, при этом состоянии существует как широкая генетическая гетерогенность, так и вариабельная фенотипическая выраженность.</p></abstract><trans-abstract xml:lang="en"><p>According to reports, patients with a number exceeding 150 with growth hormone receptor deficiency (HSCI) are mainly living in the Mediterranean region, with the exception of 7 patients from the Indian subcontinent. In Israel and Ecuador, the highest population concentrations of patients with HSCG are noted. For both of these places of population concentrations, incest is typical; there are also reports of a similar phenomenon in sporadic cases from other places. As with any hereditary disorders, apparently, in this condition there is both wide genetic heterogeneity and variable phenotypic expression.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Синдром Ларона</kwd><kwd>ИРФ-1</kwd><kwd>Рост</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Larone Syndrome</kwd><kwd>IGF-1</kwd><kwd>Growth</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">Savage М. О., Chatelain Р. G., Preece М. A. et al. // Acta paediat. scand.— 1991.—• Suppl. 377.—P. 87—90.</mixed-citation><mixed-citation xml:lang="en">Savage М. О., Chatelain Р. G., Preece М. A. et al. // Acta paediat. scand.— 1991.—• Suppl. 377.—P. 87—90.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Laron Z. // Advances in Internal Medicine / Eds H. 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