dc.contributor.author | Celik, Ahmet | |
dc.contributor.author | Papuçcu, Emre Göksan | |
dc.contributor.author | Kavak, Nede Destina | |
dc.contributor.author | Arslanca, Tufan | |
dc.date.accessioned | 2023-11-16T18:24:36Z | |
dc.date.available | 2023-11-16T18:24:36Z | |
dc.date.issued | 2022 | |
dc.identifier.issn | 2148-8274 | |
dc.identifier.issn | 2587-0084 | |
dc.identifier.uri | https://doi.org/10.24074/tjrms.2021-87410 | |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/1165422 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14065/5408 | |
dc.description.abstract | Antithrombin-3 (AT-3) is a natural anticoagulant that inhibits thrombin, activated factor X and other serine proteases in the coagulation cascade, and its activity accelerated more than 1000-fold by heparin binding. Congenital AT-3 deficiency is inherited as an autosomal dominant trait and affects less than 0.2% of the general population.1 This deficiency is considered to be a high-risk thromboembolic condition, with an odds ratio venous thromboembolism (VTE) of 16.3 compared with individuals with a nonthrombophilic status.1 In this case report, succesfull management and delivery of a congenital AT-3 deficient pregnant woman was extensively discussed along with the lşterature findinds. | en_US |
dc.language.iso | eng | en_US |
dc.relation.ispartof | Türk üreme tıbbı ve cerrahisi dergisi (Online) | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | Succesfull Management of Pregnancy Complicated with Congenital AT-3 Deficiency | en_US |
dc.type | article | en_US |
dc.department | Ufuk Üniversitesi | en_US |
dc.identifier.doi | 10.24074/tjrms.2021-87410 | |
dc.identifier.volume | 6 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 142 | en_US |
dc.identifier.endpage | 144 | en_US |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.trdizinid | 1165422 | en_US] |