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

被引:2
作者
Bulut, Ozgul [1 ]
Ince, Zeynep [1 ]
Uzunhan, Ozan [1 ]
Coban, Asuman [1 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Pediat, Div Neonatol, Istanbul, Turkey
关键词
factor V Leiden; mutations; newborn; prenatal thrombosis; prothrombin gene; VENOUS THROMBOSIS; RISK-FACTORS; REGISTRY; CARRIER;
D O I
10.1097/MBC.0000000000000686
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:220 / 222
页数:3
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