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Laurence-Moon-Biedl syndrome with vaginal atresia

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dc.contributor.author Kara, I.G.
dc.contributor.author Düzcan, F.
dc.contributor.author Aktan, E.
dc.date.accessioned 2019-08-16T11:44:52Z
dc.date.available 2019-08-16T11:44:52Z
dc.date.issued 2002
dc.identifier.issn 02844311 (ISSN)
dc.identifier.uri http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/5329
dc.description.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.
dc.language.iso English
dc.relation.isversionof 10.1080/028443102320791879
dc.subject Laurence-Moon-Biedl syndrome
dc.subject Vaginal atresia
dc.subject adolescent
dc.subject article
dc.subject astigmatism
dc.subject autosomal recessive inheritance
dc.subject Bardet Biedl syndrome
dc.subject brachydactyly
dc.subject case report
dc.subject clinical feature
dc.subject cryptorchism
dc.subject dizygotic twins
dc.subject female
dc.subject human
dc.subject hysterectomy
dc.subject karyotype 46,XX
dc.subject micropenis
dc.subject obesity
dc.subject polydactyly
dc.subject primary amenorrhea
dc.subject sibling
dc.subject uterine cervix disease
dc.subject vagina atresia
dc.subject vagina reconstruction
dc.subject visual disorder
dc.subject Adolescent
dc.subject Cervix Uteri
dc.subject Female
dc.subject Humans
dc.subject Hysterectomy
dc.subject Laurence-Moon Syndrome
dc.subject Pedigree
dc.subject Surgically-Created Structures
dc.subject Vagina
dc.title Laurence-Moon-Biedl syndrome with vaginal atresia
dc.type Article
dc.relation.journal Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery
dc.identifier.volume 36
dc.identifier.issue 5
dc.identifier.startpage 309
dc.identifier.endpage 311
dc.identifier.index Scopus


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