﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Nickan Research Institute</PublisherName>
      <JournalTitle>Journal of Parathyroid Disease</JournalTitle>
      <Issn>2345-6558</Issn>
      <Volume>11</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2023</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Hypocalcemia in thalassemia major patients requires an extra-careful approach</ArticleTitle>
    <FirstPage>e11203</FirstPage>
    <LastPage>e11203</LastPage>
    <ELocationID EIdType="doi">10.34172/jpd.2023.11203</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Bahadoram</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-7106-9799</Identifier>
      </Author>
      <Author>
        <FirstName>Bijan</FirstName>
        <LastName>Keikhaei</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-3087-7650</Identifier>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Davoodi</LastName>
      </Author>
      <Author>
        <FirstName>Najmeh</FirstName>
        <LastName>Nameh Goshay Fard</LastName>
      </Author>
      <Author>
        <FirstName>Pouria</FirstName>
        <LastName>Ghiasi</LastName>
      </Author>
      <Author>
        <FirstName>Esma'il</FirstName>
        <LastName>Akade</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-7722-0165</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>LETTER</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jpd.2023.11203</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>03</Month>
        <Day>17</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>05</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <Abstract>Thalassemia is a hematological disorder caused by a gene mutation that leads to defective synthesis of hemoglobin complex. One of the complications of thalassemia is hypocalcemia which is presented with paresthesia, muscle spasm, low-serum calcium, and intracranial calcification. Hypocalcemia can affect thalassemic patients via various mechanisms. Blood transfusion-related and transfusion-independent iron overload, drug side effects, vitamin D3 deficiency, and genetic disorders and polymorphisms are among the etiologies of hypocalcemia in major thalassemia. A careful approach to the differential etiology of this phenomenon is crucial for a resultful treatment.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Hematological disorders</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Thalassemia treatment</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Resistant hypocalcemia</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Vitamin D</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Laboratory tests</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>