<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Razi Journal of Medical Sciences</title>
<title_fa>مجله علوم پزشکی رازی</title_fa>
<short_title>RJMS</short_title>
<subject>Medical Sciences</subject>
<web_url>http://rjms.iums.ac.ir</web_url>
<journal_hbi_system_id>39</journal_hbi_system_id>
<journal_hbi_system_user>journal39</journal_hbi_system_user>
<journal_id_issn>2228-7043</journal_id_issn>
<journal_id_issn_online>2228-7051</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi></journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1381</year>
	<month>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2003</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>9</volume>
<number>32</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>سندرم شبه اسکلرودرمی معرفی یک بیمار نادر (سندرم ورنر)</title_fa>
	<title>SCLERODERMA-LIKE SYNDROM (WERNER’S SYNDROM) “A RARE CASE REPORT”</title>
	<subject_fa>روماتولوژی</subject_fa>
	<subject>Rheumatology</subject>
	<content_type_fa>موردنگاري</content_type_fa>
	<content_type>case report</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;span style=&quot;FONT-FAMILY: &quot;Times New Roman&quot;,&quot;serif&quot; FONT-SIZE: 12pt mso-fareast-font-family: 'Times New Roman' mso-bidi-font-family: 'Traditional Arabic' mso-ansi-language: EN-US mso-fareast-language: EN-US mso-bidi-language: AR-SA&quot;&gt;Scleroderma-like syndromes are a group of disorders that mimic systemic sclerosis. Werner’s syndrome is a genetically inherited syndrome that can be misdiagnosed as systemic scleroderomia. The syndrome is charachterized by sclerosis or stiffening of the skin, progeris, bilatera l juvenile cataract, endocrinopathies, premature coronary artery disease, alopecia, nail plate changes, hyperpigmentation and susceptibility to malignant neoplasms. We describe a case of Werner’s syndrome who presented with chronic leg ulcer and was misdiagnosed as systemic sclerosis for many years. We stopped unnecessary treatments and chronic leg ulcer was biopsied to rule out of skin cancer and managed locally by antibiotics and daily care.&lt;/span&gt;</abstract>
	<keyword_fa>1- سندرم ورنر    2- پیری زودرس    3- سندرم شبه اسکلرودرمی    4- اسکلروز سیستمیک</keyword_fa>
	<keyword>1) Werner’s syndrome   2) Progeria   3) Scleroderma-like syndrom   4) Systemic sclerosis </keyword>
	<start_page>637</start_page>
	<end_page>642</end_page>
	<web_url>http://rjms.iums.ac.ir/browse.php?a_code=A-10-1-1055&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>M.B.</first_name>
	<middle_name></middle_name>
	<last_name>Owlia</last_name>
	<suffix></suffix>
	<first_name_fa>محمدباقر</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>اولیاء</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>3900319475328460018274</code>
	<orcid>3900319475328460018274</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>A.</first_name>
	<middle_name></middle_name>
	<last_name>Haghighi</last_name>
	<suffix></suffix>
	<first_name_fa>انوشه</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>حقیقی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>3900319475328460018275</code>
	<orcid>3900319475328460018275</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>A.</first_name>
	<middle_name></middle_name>
	<last_name>Javadzadeh</last_name>
	<suffix></suffix>
	<first_name_fa>علی</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>جوادزاده</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>3900319475328460018276</code>
	<orcid>3900319475328460018276</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
