<?xml version="1.0"?>
<Articles JournalTitle="Journal of Craniomaxillofacial Research">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Craniomaxillofacial Research</JournalTitle>
      <Issn>2345-5489</Issn>
      <Volume>4</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Ectodermal dysplasia: A report of two cases</title>
    <FirstPage>377</FirstPage>
    <LastPage>382</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mozhgan</FirstName>
        <LastName>Kazemian</LastName>
        <affiliation locale="en_US">Oral and maxillofacial surgery,Oral and Maxillofacial Diseases Research Center, Mashhad University Of Medical Sciences, Mashhad, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Farnoosh</FirstName>
        <LastName>Razmara</LastName>
        <affiliation locale="en_US">Craniomaxillofacial Research center, Tehran University of Medical Sciences, Tehran, Iran. Oral and Maxillofacial Surgery Department, School of Dentistry,Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Nafiseh</FirstName>
        <LastName>Ghadiri Moghadam</LastName>
        <affiliation locale="en_US">Dentist.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Introduction: Ectodermal dysplasia (ED) is a group of syndromes and disorders in the human body characterized by structural anomalies in the ectoderm and often associated with hair, teeth
and skin abnormalities. There are many syndromes associated with ED.
Case report: Here is a case report of two young patients with different manifestations of ectodermal dysplasia.
Conclusion: One patient was diagnosed as Rapp-Hodgkin syndrome and the other as Hypohidrotic ectodermal dysplasia, according to clinical findings.
Key words: Ectodermal dysplasia, Hypodontia, Hypohydrotia.</abstract>
    <web_url>https://jcr.tums.ac.ir/index.php/jcr/article/view/159</web_url>
    <pdf_url>https://jcr.tums.ac.ir/index.php/jcr/article/download/159/182</pdf_url>
  </Article>
</Articles>
