<?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>37</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>1999</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW</title>
    <FirstPage>123</FirstPage>
    <LastPage>127</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>P. Mansouri.</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M. R. Mortazavi  Z. Saraii Naragki</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">Keratosis follicularis spinulosa decalvans (KFSD) represents a rare, probably X-linked recessive genodermatosis, characterized by keratosis pilaris of face, trunk and extremities, followed by atrophy, cicatricial alopecia of the scalp, eyebrows and eyelashes, photophobia and corneal abnormalities. We report a rare case of KFSD and review the literature.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/1786</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/1786/1779</pdf_url>
  </Article>
</Articles>
