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Homozygous antithrombin deficiency in adolescents presenting with lower extremity thrombosis and renal complications: two case reports from Turkey.

作者信息

Sarper Nazan, Orlando Christelle, Demirsoy Uğur, Gelen Sema A, Jochmans Kristin

机构信息

*Department of Pediatrics, Division of Pediatric Hematology, Kocaeli University, Turkey †Department of Hematology, UZ Brussel Vrije Universiteit (VUB), Brussels, Belgium.

出版信息

J Pediatr Hematol Oncol. 2014 Apr;36(3):e190-2. doi: 10.1097/MPH.0000000000000033.

DOI:10.1097/MPH.0000000000000033
PMID:24072242
Abstract

We present 2 cases of lower extremity deep venous thrombosis in 2 gypsy adolescents from related families. The patients had low antithrombin activity levels and inherited homozygous antithrombin deficiency was confirmed by molecular analysis (Leu131Phe mutation). One patient had a history of nephrectomy at the age of 9 due to nonfunctioning kidney and 2 siblings died at 4 months of age. His mother had 3 fetal losses in the third trimester. The other propositus had an elder sister who suffered from postpartum deep vein thrombosis and pulmonary embolism. Heterozygous mutation was demonstrated in both parents.

摘要

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Incidence and features of thrombosis in children with inherited antithrombin deficiency.遗传性抗凝血酶缺陷儿童的血栓形成发生率及特征。
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Antithrombin deficiency in pregnancy.
妊娠期抗凝血酶缺乏症
BMJ Case Rep. 2016 May 20;2016:bcr2015213310. doi: 10.1136/bcr-2015-213310.