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Bladder Exstrophy

dc.contributor.authorAydin, Yavuz
dc.contributor.authorAKBAS, Murat
dc.contributor.authorSen, Cihat
dc.contributor.authorUludag, Seyfettin
dc.contributor.authorUludag, Sezin
dc.contributor.authorGuralp, Onur
dc.date.accessioned2021-03-06T10:06:23Z
dc.date.available2021-03-06T10:06:23Z
dc.date.issued2012
dc.identifier.citationUludag S., Guralp O., AKBAS M., Aydin Y., Sen C., Uludag S., "Bladder Exstrophy", FETAL AND PEDIATRIC PATHOLOGY, cilt.31, ss.225-229, 2012
dc.identifier.issn1551-3815
dc.identifier.othervv_1032021
dc.identifier.otherav_e8cbd067-2960-46d6-8d37-bc97fbf149b9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/152974
dc.identifier.urihttps://doi.org/10.3109/15513815.2011.650286
dc.description.abstractBladder exstrophy is a very rare congenital malformation in which the anterior wall of the bladder is absent, and the posterior wall is exposed externally. The differential diagnosis includes omphalocele, gastroschisis, and cloacal exstrophy. Ultrasound and Doppler examinations are the main diagnostic tools. Although mortality is low, termination of pregnancy should be discussed due to serious morbidities.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBiyoloji ve Biyokimya
dc.subjectPATOLOJİ
dc.titleBladder Exstrophy
dc.typeMakale
dc.relation.journalFETAL AND PEDIATRIC PATHOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume31
dc.identifier.issue4
dc.identifier.startpage225
dc.identifier.endpage229
dc.contributor.firstauthorID17464


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