<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Pejouhesh dar Pezeshki  (Research in Medicine)</title>
<title_fa>پژوهش در پزشکی</title_fa>
<short_title>Research in Medicine</short_title>
<subject>Medical Sciences</subject>
<web_url>http://pejouhesh.sbmu.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>journal1</journal_hbi_system_user>
<journal_id_issn>1735-5311</journal_id_issn>
<journal_id_issn_online>2008-0506</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>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1353</year>
	<month>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>1975</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>3</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>other</language>
	<article_id_doi></article_id_doi>
	<title_fa>سندرم پندرد «با گزارش یک مورد»</title_fa>
	<title>Pendred Syndrome: A Case Report</title>
	<subject_fa>بین رشته ای ( مدیریت آموزشی، تحقیقات آموزشی، آموزش پزشکی )</subject_fa>
	<subject>Interdisciplinary (Educational Management, Educational research, Statistics, Medical education</subject>
	<content_type_fa>مروری</content_type_fa>
	<content_type>Review</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;In this article Pendred&amp;#39;s syndrome, which is the combination of - congenital goitre with deafmutism, is discussed. This type of goitre is due to a special enzymatic defect, involving&amp;nbsp;&lt;br&gt;
a process of hormonogenesis, which is respon-&amp;middot; sible for the incorporation of iodide in the tyrosine molecule.&amp;nbsp;&lt;br&gt;
A case of pendred&amp;#39;s syndrome is presented&amp;nbsp;&lt;br&gt;
in a 16-year-old girl. This girl has never been&amp;nbsp;able to hear or speak, and has showed symp&amp;shy;toms of hypothyroidism since :the age of 13.&amp;nbsp;&lt;br&gt;
The perchlorate test which is diagnostic and Pathognomonic for the disorder of the iodi&amp;shy;nation phase of the thyroid hoi&amp;middot;mone synthesis, was performed on this girl. The test revealed a result that was characteristic of the Pendred&amp;#39;s syndrome. In addttion an audiogramm test showed an inability to percieve high tones.&amp;nbsp;&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword></keyword>
	<start_page>210</start_page>
	<end_page>216</end_page>
	<web_url>http://pejouhesh.sbmu.ac.ir/browse.php?a_code=A-10-3973-115&amp;slc_lang=other&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Parviz</first_name>
	<middle_name></middle_name>
	<last_name>Moazami</last_name>
	<suffix></suffix>
	<first_name_fa>پرویز</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>معظمی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460020636</code>
	<orcid>100319475328460020636</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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