Literature DB >> 29194072

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.

Ozgul Bulut1, Zeynep Ince, Ozan Uzunhan, Asuman Coban.   

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.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29194072     DOI: 10.1097/MBC.0000000000000686

Source DB:  PubMed          Journal:  Blood Coagul Fibrinolysis        ISSN: 0957-5235            Impact factor:   1.276


  1 in total

1.  Three-factorial Genetic Thrombophilia with Recurrent Thrombotic Events in a Saudi Patient: A Case Report.

Authors:  Osama A Al Sultan; Eman A Al Ibrahim
Journal:  Saudi J Med Med Sci       Date:  2020-08-20
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.