妇儿健康导刊2024，Vol.3Issue(13)：79-82,4.
妊娠合并遗传性纤维蛋白原缺乏症并发胎盘早剥1例报道
A case report of pregnancy complicated with hereditary fibrinogen deficiency and placental abruption
摘要
Abstract
Hereditary fibrinogen deficiency is a rare autosomal genetic disease,laboratory examination mainly for fibrinogen levels drop,genetic testing is the gold standard in the diagnosis of hereditary fibrinogen deficiency.Pregnancy complicated with hereditary fibrinogen deficiency is prone to abortion,placental abruption,postpartum hemorrhage,etc.During pregnancy,regular prenatal examination should be performed to monitor the coagulation function and pay attention to the changes of various indicators,observe whether there is abortion and placental abruption,and give alternative treatment if necessary.Comprehensive evaluation and choose the way of delivery,to reduce adverse pregnancy outcome and the prevention and treatment of postpartum hemorrhage.A case of pregnancy complicated with hereditary fibrinogen deficiency and placental abruption in Langfang Aidebao Hospital was retrospectively analyzed,and the diagnosis and treatment of pregnancy complicated with hereditary fibrinogen deficiency were analyzed combined with literature.关键词
妊娠合并遗传性纤维蛋白原缺乏症/胎盘早剥/产后出血Key words
Pregnancy complicated with hereditary fibrinogen deficiency/Placental abruption/Postpartum hemorrhage分类
医药卫生引用本文复制引用
姚佳,谢立惠,高飞,刘静,李川..妊娠合并遗传性纤维蛋白原缺乏症并发胎盘早剥1例报道[J].妇儿健康导刊,2024,3(13):79-82,4.基金项目
廊坊市科学技术研究与发展计划自筹经费项目(2022013024). （2022013024）
