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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">555</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2021-20-3-156-157</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Red cell distribution width as a differential parameter between iron deficiency anemia and a-thalassemia: an empirical approach</article-title><trans-title-group xml:lang="ru"><trans-title>Red cell distribution width as a differential parameter between iron deficiency anemia and a-thalassemia: an empirical approach</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Keikhaei</surname><given-names>Bijan</given-names></name><address><country country="IR">Iran, Islamic Republic of</country></address><bio><p>Ahvaz</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Bahadoram</surname><given-names>Mohammad</given-names></name><address><country country="IR">Iran, Islamic Republic of</country></address><bio><p>Ahvaz</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Mahmoudian-Sani</surname><given-names>Mohammad-Reza</given-names></name><address><country country="IR">Iran, Islamic Republic of</country></address><bio xml:lang="en"><p><bold>Mohammad-Reza Mahmoudian-Sani</bold>, Assistant Professor of Molecular Medicine School of Medicine </p><p>Ahvaz </p></bio><bio xml:lang="ru"><p><bold>Mohammad-Reza Mahmoudian-Sani</bold>, Assistant Professor of Molecular Medicine School </p><p>Ahvaz</p></bio><email>mohamadsani495@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Bahadoram</surname><given-names>Sara</given-names></name><address><country country="IR">Iran, Islamic Republic of</country></address><bio><p>Ahvaz</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Thalassemia and Hemoglobinopathy Research Center, Research Institute of Health, Ahvaz Jundishapur University of Medical Sciences</institution></aff><pub-date date-type="pub" iso-8601-date="2021-10-08" publication-format="electronic"><day>08</day><month>10</month><year>2021</year></pub-date><volume>20</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>156</fpage><lpage>157</lpage><history><date date-type="received" iso-8601-date="2021-10-08"><day>08</day><month>10</month><year>2021</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2021, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2021, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/555">https://hemoncim.com/jour/article/view/555</self-uri><abstract xml:lang="en"><p>Iron deficiency anemia (IDA) and thalassemia minor are the most common hypochromic microcytic anemias in the world. Different formulas have been proposed to differentiate IDA from beta thalassemia minor. However, yet no formula has been proposed to differentiate IDA from alpha thalassemia minor, and Hb electrophoresis is not helpful in this hemoglobinopathy. Red cell distribution width (RDW) as indicator of changes in red blood cell size is primarily employed to differentiate IDA from other microcytic anemias. An empirical approach involving iron therapy over 1 month has shown that an increase in Hb concentration by 1 g/dL over this period is indicative of IDA, while no changes in Hb concentration are suggestive of alpha thalassemia. RDW measured after iron therapy in order to differentiate IDA and related disorders from alpha thalassemia is a better index than an increased reticulocyte count. Due to the high prevalence of IDA and costly and time-consuming nature of specific diagnostic tests, the RDW index is considered as a very sensitive and cost-effective tool in the differential diagnosis of IDA.</p></abstract><trans-abstract xml:lang="ru"><p>Iron deficiency anemia (IDA) and thalassemia minor are the most common hypochromic microcytic anemias in the world. Different formulas have been proposed to differentiate IDA from beta thalassemia minor. However, yet no formula has been proposed to differentiate IDA from alpha thalassemia minor, and Hb electrophoresis is not helpful in this hemoglobinopathy. Red cell distribution width (RDW) as indicator of changes in red blood cell size is primarily employed to differentiate IDA from other microcytic anemias. An empirical approach involving iron therapy over 1 month has shown that an increase in Hb concentration by 1 g/dL over this period is indicative of IDA, while no changes in Hb concentration are suggestive of alpha thalassemia. RDW measured after iron therapy in order to differentiate IDA and related disorders from alpha thalassemia is a better index than an increased reticulocyte count. Due to the high prevalence of IDA and costly and time-consuming nature of specific diagnostic tests, the RDW index is considered as a very sensitive and cost-effective tool in the differential diagnosis of IDA.</p></trans-abstract><kwd-group xml:lang="en"><kwd>iron deficiency anemia</kwd><kwd>a-thalassemia</kwd><kwd>red cell distribution width</kwd><kwd>hypochromic microcytic anemias</kwd><kwd>b-thalassemia</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>iron deficiency anemia</kwd><kwd>a-thalassemia</kwd><kwd>red cell distribution width</kwd><kwd>hypochromic microcytic anemias</kwd><kwd>b-thalassemia</kwd></kwd-group><funding-group><funding-statement xml:lang="en">This study was financially supported by Ahvaz Jundishapur University of Medical Sciences.</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Tari K., Atashi A., Karami F., Shahjahani M. 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