dc.contributor.author | Bulut, Ozgul | |
dc.contributor.author | Coban, Asuman | |
dc.contributor.author | Ince, Zeynep | |
dc.contributor.author | Uzunhan, Ozan | |
dc.date.accessioned | 2021-03-02T22:51:28Z | |
dc.date.available | 2021-03-02T22:51:28Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Bulut O., Ince Z., Uzunhan O., Coban A., "Prenatal thrombosis of renal veins and the inferior vena cava in a newborn with double heterozygosity for the factor V Leiden and prothrombin gene G20210A mutations: a case report.", Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, cilt.29, sa.2, ss.220-222, 2018 | |
dc.identifier.issn | 0957-5235 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_0f207bc2-5e0a-46d1-a3bd-5622fc80b386 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/15697 | |
dc.identifier.uri | https://doi.org/10.1097/mbc.0000000000000686 | |
dc.description.abstract | Renal vein thrombosis in a neonate is a rare but well recognized condition with low mortality but high morbidity. The cause has not been explained clearly yet but is probably a multifactorial process that includes inherited prothrombotic abnormalities. Antenatal onset of renal vein thrombosis is important due to the increased risk for permanent organ damage. We report a case of prenatal thrombosis of the renal veins and the inferior vena cava in a newborn with double heterozygosity for factor V Leiden and prothrombin gene mutations who had persistently impaired renal function requiring chronic peritoneal dialysis. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved. | |
dc.language.iso | eng | |
dc.subject | İç Hastalıkları | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Hematoloji | |
dc.subject | Tıp | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | HEMATOLOJİ | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.title | Prenatal thrombosis of renal veins and the inferior vena cava in a newborn with double heterozygosity for the factor V Leiden and prothrombin gene G20210A mutations: a case report. | |
dc.type | Makale | |
dc.relation.journal | Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 29 | |
dc.identifier.issue | 2 | |
dc.identifier.startpage | 220 | |
dc.identifier.endpage | 222 | |
dc.contributor.firstauthorID | 251893 | |