TRUE COMPLETE DIPHALLIA
dc.contributor.author | ZOLFAGHARI, A | |
dc.contributor.author | POURISSA, M | |
dc.contributor.author | HAJIALILOU, S | |
dc.contributor.author | AMJADI, M | |
dc.date.accessioned | 2018-08-26T08:31:43Z | |
dc.date.available | 2018-08-26T08:31:43Z | |
dc.date.issued | 1995 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52193 | |
dc.description.abstract | In 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. | |
dc.language.iso | English | |
dc.relation.ispartof | SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY | |
dc.subject | DIPHALLIA | |
dc.subject | CONGENITAL MALFORMATIONS | |
dc.title | TRUE COMPLETE DIPHALLIA | |
dc.type | Note | |
dc.citation.volume | 29 | |
dc.citation.issue | 2 | |
dc.citation.spage | 233 | |
dc.citation.epage | 235 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.3109/00365599509180570 |
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