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Depletion of Specific Cell Populations by Complement Depletion
Published on: February 5, 2010
在努南综合征中,凝血因子缺乏和异常出血
M Sharland1, M A Patton, S Talbot
1South West Thames Regional Genetics Service, St George's Hospital Medical School, London, UK.
Lancet (London, England)
|January 4, 1992
概括
努南综合征患者经常因为内在凝血路缺陷而出现出血问题. 这些出血障碍,包括因子缺乏症,表明在努南综合征中存在自体遗传联系.
科学领域:
- 遗传学 遗传学是一种遗传学.
- 血液学 血液学 血液学
- 儿科 儿科 儿科
背景情况:
- 努南综合征是一种自体主导性疾病.
- 关键特征包括异形面部,先天性心脏病和矮身.
- 异常出血在患者中曾经有过事报告.
研究的目的:
- 为了研究患有努南综合征的个体的凝血因子缺陷.
- 为了确定出血异常的患病率和性质.
- 探索这种情况中出血倾向的遗传基础.
主要方法:
- 研究了72名诺南综合征患者 (37名男性,35名女性).
- 评估了异常伤或出血的病史.
- 进行了凝血试验,包括激活的部分血栓塑时间.
- 在内在途径中确定了特定的凝血因子缺陷.
主要成果:
- 65%的患者报告有异常出血史.
- 40%的人表现出延长的激活部分血栓形成时间.
- 50%的人存在内在通路因子 (XI,XII,VIII) 的缺陷.
- 在出血史和因子缺陷之间观察到较差的相关性.
- 在患有努南综合征的亲属中发现了类似的凝血缺陷.
结论:
- 努南综合征与内在途径凝血因子缺乏有关.
- 这些出血异常表明凝血级联的自身体调节.
- 需要进一步的研究来阐明涉及的遗传机制.
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