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dc.contributor.authorOztunc, Funda
dc.contributor.authorOzel, Aysegul
dc.contributor.authorUludag, Seyfettin
dc.contributor.authorMadazli, Riza
dc.contributor.authorKizilkilic, Osman
dc.contributor.authorErenel, Hakan
dc.contributor.authorComunoglu, Nil
dc.date.accessioned2021-03-05T13:43:40Z
dc.date.available2021-03-05T13:43:40Z
dc.date.issued2018
dc.identifier.citationErenel H., Ozel A., Oztunc F., Kizilkilic O., Comunoglu N., Uludag S., Madazli R., "Antenatal Diagnosis of Fetal Retinoid Syndrome at 20 Weeks of Gestation: A Case Report", FETAL AND PEDIATRIC PATHOLOGY, cilt.37, ss.282-286, 2018
dc.identifier.issn1551-3815
dc.identifier.othervv_1032021
dc.identifier.otherav_b39afecc-d2ce-41a2-9adc-11f2f94ea7a8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/119629
dc.identifier.urihttps://doi.org/10.1080/15513815.2018.1472354
dc.description.abstractIntroduction: Isotretinoin, a synthetic derivative of vitamin A, is one of the most potent human teratogens, and is mainly utilized for the treatment of severe recalcitrant nodular acne. Retinoic acid embryopathy is well defined in the literature. Case Report: The mother was referred for a fetal posterior fossa abnormality, first detected at 20 weeks of gestation. The mother used isotretinoin until 18 weeks gestation. Ultrasound examination revealed hypertelorism, cerebellar hypoplasia, vermian agenesis, truncus arteriosus, anotia, thymic aplasia, corpus callosum hypoplasia. An intrauterine diagnosis of fetal retinoid syndrome was confirmed by fetopsy after termination of pregnancy. Conclusion: The typical findings of fetal retinoid syndrome can be visualized with ultrasound in early second trimester.
dc.language.isoeng
dc.subjectPatoloji
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleAntenatal Diagnosis of Fetal Retinoid Syndrome at 20 Weeks of Gestation: A Case Report
dc.typeMakale
dc.relation.journalFETAL AND PEDIATRIC PATHOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume37
dc.identifier.issue4
dc.identifier.startpage282
dc.identifier.endpage286
dc.contributor.firstauthorID248861


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