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https://hdl.handle.net/11499/5329| Title: | Laurence-Moon-Biedl syndrome with vaginal atresia | Authors: | Kara, İnci Gökalan Düzcan, Füsun Aktan, Erdal |
Keywords: | Laurence-Moon-Biedl syndrome Vaginal atresia adolescent article astigmatism autosomal recessive inheritance Bardet Biedl syndrome brachydactyly case report clinical feature cryptorchism dizygotic twins female human hysterectomy karyotype 46,XX micropenis obesity polydactyly primary amenorrhea sibling uterine cervix disease vagina atresia vagina reconstruction visual disorder Adolescent Cervix Uteri Female Humans Hysterectomy Laurence-Moon Syndrome Pedigree Surgically-Created Structures Vagina |
Abstract: | A 15-year-old girl presented with the rare Laurence-Moon-Biedl syndrome, accompanied by vaginal atresia, and cervical dysgenesis. She was treated by hysterectomy and construction of a neovagina with bilateral pudendal thigh flaps. Two brothers and a sister (one of twins) were unaffected but the remaining brother also had the disease. | URI: | https://hdl.handle.net/11499/5329 https://doi.org/10.1080/028443102320791879 |
ISSN: | 0284-4311 |
| Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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