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Craniofacial anomalies associated with hypospadias. Description of a hospital based population in South America

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dc.creatorFernandez, Nicolas
dc.creatorEscobar, Rebeca
dc.creatorZarante, Ignacio
dc.creator.googleFernandez, Nicolasspa
dc.creator.googleEscobar, Rebecaspa
dc.creator.googleZarante, Ignaciospa
dc.date.accessioned2020-04-02T02:52:08Z
dc.date.available2020-04-02T02:52:08Z
dc.date.created2016-08
dc.date.issued2016
dc.description.abstractIntroduction: Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing an increase of prevalence of hypospadias. Association of craniofacial malformations in patients diagnosed with hypospadias is rare. The aim of this study is to describe the association between hypospadias and craniofacial congenital anomalies. Materials and Methods: A retrospective review of the Latin-American collaborative study of congenital malformations (ECLAMC) data was performed between January 1982 and December 2011. We included children diagnosed with associated hypospadias and among them we selected those that were associated with any craniofacial congenital anomaly. Results: Global prevalence was 11.3 per 10.000 newborns. In this population a total of 809 patients with 1117 associated anomalies were identified. On average there were 1.7 anomalies per patient. Facial anomalies were present in 13.2%. The most commonly major facial anomaly associated to hypospadias was cleft lip/palate with 52 cases. We identified that 18% have an association with other anomalies, and found an association between craniofacial anomalies and hypospadias in 0.59 cases/10.000 newborns. Discussion: Hypospadias is the most common congenital anomaly affecting the genitals. Its association with other anomalies is rare. It has been reported that other malformations occur in 29.3% of the cases with hypospadias. The more proximal the meatus, the higher the risk for having another associated anomaly. Conclusion: Associated hypospadias are rare, and it is important to identify the concurrent occurrence of craniofacial anomalies to better treat patients that might need a multidisciplinary approach.eng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1590/S1677-5538.IBJU.2015.0568
dc.identifier.issn1677-5538
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/21394
dc.language.isoengspa
dc.relation.citationEndPage797
dc.relation.citationIssueNo. 4
dc.relation.citationStartPage793
dc.relation.citationTitleInternational Braz J Urol
dc.relation.citationVolumeVol. 42
dc.relation.ispartofInternational Braz J Urol, ISSN: 1677-5538 Vol. 42, No. 4 (2016) pp. 793-797spa
dc.relation.urihttp://www.scielo.br/pdf/ibju/v42n4/1677-5538-ibju-42-04-0793.pdfspa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto Completo)spa
dc.source.instnameinstname:Universidad del Rosario
dc.source.reponamereponame:Repositorio Institucional EdocUR
dc.subjectclinical trialspa
dc.subjectCraniofacial Abnormalitiesspa
dc.subjecthealth surveyspa
dc.subjecthypospadiasspa
dc.subjectmalespa
dc.subjectmulticenter studyspa
dc.subjectnewbornspa
dc.subjectSouth Americaspa
dc.subjectCraniofacial Abnormalitiesspa
dc.subjectHypospadiasspa
dc.subjectMalespa
dc.subjectPopulation Surveillancespa
dc.subjectPrevalencespa
dc.subjectSouth Americaspa
dc.subjectHipospadiasspa
dc.subjectCraneofacial anormalidadesspa
dc.subjectSudamericaspa
dc.subjectGrupos de poblaciónspa
dc.subject.ddcEnfermedadesspa
dc.subject.keywordHypospadiasspa
dc.subject.keywordCraniofacial abnormalitiesspa
dc.subject.keywordSouth Americaspa
dc.subject.keywordhumanspa
dc.subject.keywordprevalencespa
dc.subject.keywordHumansspa
dc.subject.keywordInfanteng
dc.subject.lembHipospadiasspa
dc.subject.lembAnomalías congénitasspa
dc.titleCraniofacial anomalies associated with hypospadias. Description of a hospital based population in South Americaspa
dc.typearticleeng
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.type.spaArtículospa
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