<?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>33</Volume>
      <Issue>1-2</Issue>
      <PubDate PubStatus="epublish">
        <Year>1995</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">PHAKOMATOSIS PIGMENTOVASCULARIS: REPORT OF A CASE</title>
    <FirstPage>35</FirstPage>
    <LastPage>38</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>Mostafa Mirshams-Shahshahani</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>Zahra Safaii-Naraghi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>&#xA0; Mohammad-Reza Mortazavi</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 present study introduces a rare case of phakomatosispigmenJovascularis, which is charaderiud by the existence ofpigmentary naevus ond vascular naevus. Until 1985, 63 cases ofthis syndrome have been reported, mostly in Japon (56 cases). This is the first case of phakomatosis pigmentovascularis, reported in Iran.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/1661</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/1661/1654</pdf_url>
  </Article>
</Articles>
