<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>44</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2006</Year>
        <Month>04</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">"CONGENTIAL PANHYPOPITUITARISM ASSOCIATED WITH IMPAIRED LIVER FUNCTION TESTS AND CONGENITAL HEART DISEASE"</title>
    <FirstPage>155</FirstPage>
    <LastPage>156</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>Z. Khalili-Matinzadeh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The term congenital hypopituitarism defines deficiency of all of the pituitary hormones.
Hypoglycemia and microphallus (in males) are common findings, and some infants have shown
evidence of the neonatal hepatitis syndrome. We report a case of congenital panhypopituitarism with deficiency of six major hormones and association with severe hypoglycemia, impaired liver function tests and congenital heart disease.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/3159</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/3159/3139</pdf_url>
  </Article>
</Articles>
