先天性无纤维蛋白原血症表现为产前颅内出血：病例报告。
Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report.
机构信息
Amrita Institute of Medical Sciences (AIMS), Kochi, Kerala, India.
出版信息
Ital J Pediatr. 2010 Jan 5;36:1. doi: 10.1186/1824-7288-36-1.
Abstract
Congenital afibrinogenemia is a very rare inherited coagulation disorder, characterized by virtual absence of plasma fibrinogen (factor I). There are only about 250 cases reported in the world literature 1. We describe a case of congenital afibrinogenemia which presented as an antenatally detected intracranial bleed.
摘要
先天性无纤维蛋白原血症是一种非常罕见的遗传性凝血障碍，其特征是血浆纤维蛋白原（因子 I）几乎完全缺失。全世界文献中仅报道了约 250 例病例。1 我们描述了 1 例以产前发现的颅内出血为表现的先天性无纤维蛋白原血症病例。
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