<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Clinical Care and Skills</title>
<title_fa>مجله مهارت‌ها و مراقبت‌های بالینی</title_fa>
<short_title>J Clinic Care Skill</short_title>
<subject>Medical Sciences</subject>
<web_url>http://jccs.yums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2645-7687</journal_id_issn>
<journal_id_issn_online>2645-7687</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.58209/jccs</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>1403</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2024</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<volume>5</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Unilateral Multiple Renal Congenital Anomalies; A Case Report</title>
	<subject_fa>General Nursing</subject_fa>
	<subject>General Nursing</subject>
	<content_type_fa>گزارش مورد/موارد</content_type_fa>
	<content_type>Case/Series Report</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;span style=&quot;font-family:Calibri,sans-serif&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt;&lt;span style=&quot;color:#44546a&quot;&gt;Aims:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt; The urinary tract is a site for common anomalies. Ureteropelvic junction obstruction and double collecting system are among the most common anomalies in the body, but gathering all of these anomalies reported in our patient and being unilateral may be a rare entity. Hereby, we report a case with such a rare condition.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;span style=&quot;font-family:Calibri,sans-serif&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt;&lt;span style=&quot;color:#44546a&quot;&gt;Patient &amp; Methods:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt; The patient is a 19-year-old army male who presented with left lower quadrant abdominal pain after blunt abdominal trauma, accompanied by gross hematuria. &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;span style=&quot;font-family:Calibri,sans-serif&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt;&lt;span style=&quot;color:#44546a&quot;&gt;Findings:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt; Ultrasonography suggested an ectopic pelvic left kidney with hydronephrosis and ureteropelvic junction obstruction with distal ureteral dilatation. Exploration was done through a Gibson&amp;rsquo;s retroperitoneal incision, and pyeloplasty accompanied by ureteroneocystostomy was carried out. &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;span style=&quot;font-family:Calibri,sans-serif&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt;&lt;span style=&quot;color:#44546a&quot;&gt;Conclusion:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;&lt;span cambria=&quot;&quot; style=&quot;font-family:&quot;&gt;The collection of unilateral renal ectopia, double collecting system, lower moiety ureteropelvic junction obstruction, and finally ending to a common ureter with ureterovesical junction obstruction, seems to be a rare condition, but we found all of these in a young male.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Congenital Anomalies,Kidney,Urinary Tract System,</keyword>
	<start_page>77</start_page>
	<end_page>80</end_page>
	<web_url>http://jccs.yums.ac.ir/browse.php?a_code=A-10-248-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name> S.M.R.</first_name>
	<middle_name></middle_name>
	<last_name>Rabani</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846004008</code>
	<orcid>10031947532846004008</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Departments of Urology, Faculty of Medicine, Yasuj University of Medical Sciences, Yasuj, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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