先天性因子V缺乏症的迟发性表现——一例报告
Late presentation of congenital factor V deficiency--a case report.
作者信息
Pavithran K, Sankar S, Thomas M
机构信息
Medical College Hospital, Thiruvananthapuram-695011.
出版信息
Indian J Med Sci. 2001 May;55(5):271-2.
PMID:11641920
Abstract
Congenital factor deficiency is a rare coagulation disorder, which is inherited in an autosomal recessive manner. The severity of bleeding symptoms in general is only partially related to the degree of factor V deficiency in plasma. In this report, a boy presenting with hemarthrosis in his late adolescence due to congenital factor V deficiency is reported.
摘要
先天性因子缺乏是一种罕见的凝血障碍，以常染色体隐性方式遗传。一般来说，出血症状的严重程度仅部分与血浆中因子V缺乏的程度有关。在本报告中，报道了一名因先天性因子V缺乏在青春期后期出现关节积血的男孩。
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