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True complete diphallia: Case report

dc.contributor.authorZolfaghari, A
dc.contributor.authorPourissa, M
dc.contributor.authorHajialilou, S
dc.contributor.authorAmjadi, M
dc.date.accessioned2018-08-26T09:43:39Z
dc.date.available2018-08-26T09:43:39Z
dc.date.issued1995
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58620
dc.description.abstractIn a case of true complete diphallia, the orthotopic penis was normal in length, shape and urethra, whereas the ectopic, perianal, penis had a blind-ending urethra, the significant distance between the two making the malformation of an extremely rare type. Right renal agenesis and orthopaedic malformations were also present. © 1995 Informa UK Ltd.
dc.language.isoEnglish
dc.relation.ispartofScandinavian Journal of Urology and Nephrology
dc.subjectarticle
dc.subjectcase report
dc.subjecthuman
dc.subjectinfant
dc.subjectpenis
dc.subjectpenis duplication
dc.subjectpriority journal
dc.subjectAbnormalities, Multiple
dc.subjectAnus
dc.subjectCase Report
dc.subjectHernia, Inguinal
dc.subjectHuman
dc.subjectInfant
dc.subjectKidney
dc.subjectMale
dc.subjectPenis
dc.subjectUrethra
dc.titleTrue complete diphallia: Case report
dc.typeArticle
dc.citation.volume29
dc.citation.issue2
dc.citation.spage233
dc.citation.epage235
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.3109/00365599509180570


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