因子V缺乏症：一种隐匿的表现。

Factor v deficiency: a subtle presentation.

作者信息

Sanklecha Mukesh Uttamchand, Sundaresan Suba, Charde Vivek

机构信息

Department of Pediatrics, Bombay Hospital Institute of Medical Sciences, Mumbai, India,

出版信息

Indian J Pediatr. 2014 Mar;81(3):283-4. doi: 10.1007/s12098-013-1180-y. Epub 2013 Jul 24.

DOI:10.1007/s12098-013-1180-y

PMID:23881482

Abstract

Congenital factor V deficiency (also known as labile factor or proaccelerin) is a rather uncommon [1:1000,000] inherited coagulopathy (autosomal recessive inheritance). Affected patients become symptomatic in early childhood with spontaneous or post-traumatic bleeding complications. The authors report an infant who presented with a much feared complication of the same probably as a neonatal presentation.

摘要

先天性因子V缺乏症（也称为不稳定因子或前加速素）是一种相当罕见的[1:1000000]遗传性凝血病（常染色体隐性遗传）。受影响的患者在幼儿期就会出现症状，伴有自发性或创伤后出血并发症。作者报告了一名婴儿，可能作为新生儿表现出了同样令人担忧的并发症。