<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Allergy, Asthma and Immunology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>06</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The Clinical Approach toward Hereditary Persistence of Fetal Hemoglobin:  A Case Report</title>
    <FirstPage>364</FirstPage>
    <LastPage>368</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Afshin</FirstName>
        <LastName>Ghaderi</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Hematology and Medical Oncology Ward, Yasuj University of Medical Sciences, Yasuj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Tahereh</FirstName>
        <LastName>Bakhtiari</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Saeid</FirstName>
        <LastName>Jokar</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Shahids Rajaee Hospital of Gachsaran, Yasuj University of Medical Sciences, Yasuj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abbas</FirstName>
        <LastName>Eshraghi</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Qom University of Medical Sciences, Qom, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>09</Month>
        <Day>05</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>10</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Fetal hemoglobin is the principal hemoglobin in the human fetus, and the adult levels of fetal hemoglobin (HbF) are less than 1% of total hemoglobin. A steady increase of HbF in patients with hereditary persistence of fetal hemoglobin (HPFH) is associated with complications. The present report describes HPFH in a 26-year-old man with emphasis on its hemoglobin electrophoresis. The patient was admitted with complaints of recurrent weakness and lethargy, weight loss, abdominal pain, and dyspepsia. Splenectomy was planned due to massive splenomegaly and gastrointestinal complications. Ultimately, &#xA0;electrophoresis confirmed the diagnosis of HPFH.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3348</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3348/1803</pdf_url>
  </Article>
</Articles>
