<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>jmedicalcasereports</PublisherName> <JournalTitle>Frontiers in Medical Case Reports</JournalTitle> <PISSN>I</PISSN> <EISSN>S</EISSN> <Volume-Issue>Volume 2; Issue 5</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>(Sep-Oct, 2021)</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>-0001</Year> <Month>11</Month> <Day>30</Day> </PubDate> <ArticleType>Medical Case Reports</ArticleType> <ArticleTitle>Atypical 9p- Partial Deletion Syndrome: First Case in Mozambique</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>1</FirstPage> <LastPage>2</LastPage> <AuthorList> <Author> <FirstName>Hector Rafael Cespedes</FirstName> <LastName>Rodriguez</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>Valeria Isabel Muando</FirstName> <LastName>Chicamba</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI/> <Abstract/> <AbstractLanguage>English</AbstractLanguage> <Keywords>9p- Partial Deletion Syndrome,Genetic Syndromes</Keywords> <URLs> <Abstract>https://www.jmedicalcasereports.org/ubijournal-v1copy/journals/abstract.php?article_id=13315&title=Atypical 9p- Partial Deletion Syndrome: First Case in Mozambique</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References>Torres E, Monjagata N, Herreros MB, Ascurra M, Rodrand;iacute;guez S, Ayala A. Monosomand;iacute;a Parcial del Brazo Corto del Cromosoma 9. Pediatr (Asunciand;oacute;n) 2009; 36: 219–222. Alcaland;aacute; FC, Rodrand;iacute;guez MM, Casado IG, Bris LO, Fresno LS, Guerrero-Fernand;aacute;ndez J, Martand;iacute;nez-Frand;iacute;as ML, Bouthelier RG. Delecion 9p-. Disgenesia gonadal asociada a retraso mental. An Pediatr (Barc) 2010; 72: 210–214 Fernand;aacute;ndez Calderand;oacute;n E, Galand;aacute;n Gand;oacute;mez E, Carbonell Pand;eacute;rez J, Sand;aacute;enz Hurtado J, Ledesma Alcand;aacute;zar M, Cardesa Garcand;iacute;a J. Diagnand;oacute;stico del sand;iacute;ndrome 9p– al nacimiento. Una nueva observaciand;oacute;n. AnPediatr (Barc) 2004; 61: 185-196. National organization for rare disorders. Chromosome 9, Partial Monosomy 9p. On-line consultation date 2016/06/10. https://rarediseases.org/rare-diseases/chromosome-9-partial-monosomy-9p/ Sirisena ND, Wijetunge UK, de Silva R, Dissanayake VH. Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations. Case Rep Genet 2013; 2013: 785830.</References> </References> </Journal> </Article> </ArticleSet>