<?xml version="1.0" encoding="utf-8"?>
			<journal>
			<title>Iranian Journal of Neonatology</title>
			<title_fa>مجله نوزادان ایران</title_fa>
			<short_title>IJN</short_title>
			<subject>Medical Sciences</subject>
			<web_url>https://ijn.mums.ac.ir/</web_url>
			<journal_hbi_system_id>0</journal_hbi_system_id>
			<journal_hbi_system_user></journal_hbi_system_user>
			<journal_id_issn>2251-7510</journal_id_issn>
			<journal_id_issn_online>2322-2158</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>0</year>
				<month>0</month>
				<day>1</day>
			</pubdate>
			<pubdate>
				<type>gregorian</type>
				<year>2026</year>
				<month>4</month>
				<day>1</day>
			</pubdate>
			<volume>17</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_issn></article_id_issn>
				<article_id_issn_online></article_id_issn_online>
				<article_id_pubmed></article_id_pubmed>
				<article_id_pii></article_id_pii>
				<article_id_doi></article_id_doi>
				<article_id_iranmedex></article_id_iranmedex>
				<article_id_magiran></article_id_magiran>
				<article_id_sid></article_id_sid>
				<title_fa></title_fa>
				<title>Bilateral Palmar Single Transverse Crease in an Infant Girl with Ring Chromosome 13 and Multiple Facial Anomalies: A Case Report</title>
				<subject_fa></subject_fa>
				<subject></subject>
				<content_type_fa>گزارش موارد نادر</content_type_fa>
				<content_type>Case Report</content_type>
				<abstract_fa><![CDATA[]]></abstract_fa>
				<abstract><![CDATA[Background: Ring chromosome 13 is a rare cytogenetic disorder resulting from breakage and reunion of the distal ends of the chromosomal arms. The incidence of this disorder is about 1 in 58,000 live births. This syndrome usually presents with particular clinical features, including developmental delay, microcephaly, genital malformation in males, and dysmorphism, such as hypertelorism, broad nasal bridge, thin lips, up-slanting palpebral fissure, and ear anomalies.
Case Report: We report a 2-month-old girl who was referred to a clinical geneticist because of growth retardation and distinctive facial features. Her parents were consanguineous (second-cousins). The patient had a history of IUGR and was the product of a normal delivery at 39 weeks of gestation. At presentation, hypotonia, microcephaly, micrognathia, low-set ears, bilateral palmar single transverse creases (simian creases), broad nasal bridge, and thin lips were observed.
Conclusion: The karyotype revealed the presence of mosaic ring chromosome 13. This is the first report of a case of ring chromosome 13 with bilateral palmar single transverse creases.
 ]]></abstract>
				<keyword_fa></keyword_fa>
				<keyword>Cytogenetic, Microcephaly, palmar single transverse crease, Ring chromosome 13, Simian crease</keyword>
				<start_page>46</start_page>
				<end_page>49</end_page>
				<web_url>https://ijn.mums.ac.ir/article_27380.html</web_url>
			<author_list><author>
				<first_name>Mohammad</first_name>
				<middle_name></middle_name>
				<last_name>Vasei</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>mvasei@tums.ac.ir</email>
				<code>120275</code>
				<coreauthor>No</coreauthor>
				<affiliation>Gene Therapy Research Center, Digestive Diseases Research Institute, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Alireza</first_name>
				<middle_name></middle_name>
				<last_name>Biglari</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>abiglari@sina.tums.ac.ir</email>
				<code>120276</code>
				<coreauthor>No</coreauthor>
				<affiliation>Children's Medical Center, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Moeinadin</first_name>
				<middle_name></middle_name>
				<last_name>Safavi</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>moein.safavi@gmail.com</email>
				<code>120277</code>
				<coreauthor>No</coreauthor>
				<affiliation>Molecular Pathology and Cytogenetic Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Leila</first_name>
				<middle_name></middle_name>
				<last_name>Mousavi</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>leilamosavi1395@gmail.com</email>
				<code>120278</code>
				<coreauthor>No</coreauthor>
				<affiliation>Cytogenetic Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author><author>
				<first_name>Mahboobeh</first_name>
				<middle_name></middle_name>
				<last_name>Chahkandi</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>mahboobehchahkandi@gmail.com</email>
				<code>120274</code>
				<coreauthor>Yes</coreauthor>
				<affiliation>Molecular and Cytogenetic Pathology, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
				<affiliation_fa></affiliation_fa>
				 </author></author_list>
				</article>
			</articleset>
			</journal>