• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.弗留利X因子凝血障碍:近50年后
Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29.
2
Complex history of the discovery and characterization of congenital factor X deficiency.先天性因子X缺乏症的发现与特征描述的复杂历程。
Semin Thromb Hemost. 2015 Jun;41(4):359-65. doi: 10.1055/s-0034-1544000. Epub 2015 Apr 14.
3
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).在长达23.5年的连续观察期内,对128名X因子缺乏杂合子(主要是弗留利因子X缺乏症)患者与128名未受影响的家庭成员进行匹配,观察出血表现的患病率。
Eur J Haematol. 2016 Dec;97(6):547-553. doi: 10.1111/ejh.12767. Epub 2016 May 30.
4
Factor X Friuli coagulation disorder. Report of a newly recognized patient and some considerations on the frequency of the disease in the Friuli area.弗留利X因子凝血障碍。一例新确诊患者的报告及对弗留利地区该病发病率的一些思考。
Acta Haematol. 1976;56(1):27-38. doi: 10.1159/000207916.
5
Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide.因意外摄入敌鼠酮类灭鼠剂导致联合遗传性因子 VII 和因子 X 缺乏患者的诊断错误
Clin Lab. 2016 Nov 1;62(11):2253-2256. doi: 10.7754/Clin.Lab.2016.160503.
6
A family with heterozygous factor X Friuli defect outside Friuli.
Blut. 1983 Mar;46(3):149-54. doi: 10.1007/BF00320273.
7
Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X.对一名具有斯里兰卡血统的法国患者遗传性因子X缺乏症的基因分析:体外表达研究确定Gly366Ser替代是功能失调的因子X的分子基础。
Blood Coagul Fibrinolysis. 2005 Jan;16(1):9-16. doi: 10.1097/00001721-200501000-00002.
8
A new factor X defect (factor X Padua 3): a compound heterozygous between true deficiency (Gly(380)-->Arg) and an abnormality (Ser(334)-->Pro).一种新的凝血因子X缺陷(帕多瓦因子X 3型):一种真正缺乏(甘氨酸(380)→精氨酸)与一种异常(丝氨酸(334)→脯氨酸)之间的复合杂合状态。
Thromb Res. 2001 Nov 15;104(4):257-64. doi: 10.1016/s0049-3848(01)00371-1.
9
The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade.一位出血患者的凝血因子 X 激活肽中的错义 Thr211Pro 突变导致凝血级联中的分子缺陷。
Thromb Haemost. 2013 Jul;110(1):53-61. doi: 10.1160/TH13-03-0184. Epub 2013 May 16.
10
A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).一个来自阿根廷的患有X因子缺乏症的家族:由于一个新突变(Gln138Arg)与一个已知突变(Glu350Lys)的组合导致的复合杂合性。
Blood Coagul Fibrinolysis. 2016 Sep;27(6):732-6. doi: 10.1097/MBC.0000000000000563.

引用本文的文献

1
[Phylogenetic analysis and pathogenesis study of a new deletion mutation causing inherited FⅩ deficiency].[一种导致遗传性FⅩ缺乏症的新型缺失突变的系统发育分析及发病机制研究]
Zhonghua Xue Ye Xue Za Zhi. 2024 Oct 14;45(10):902-908. doi: 10.3760/cma.j.cn121090-20240506-00169.

本文引用的文献

1
Factor X and its deficiency states.
Haemophilia. 1997 Jul;3(3):159-72. doi: 10.1046/j.1365-2516.1997.00106.x.
2
Complex history of the discovery and characterization of congenital factor X deficiency.先天性因子X缺乏症的发现与特征描述的复杂历程。
Semin Thromb Hemost. 2015 Jun;41(4):359-65. doi: 10.1055/s-0034-1544000. Epub 2015 Apr 14.
3
Coagulation factor VII variants resistant to inhibitory antibodies.对抑制性抗体具有抗性的凝血因子VII变体。
Thromb Haemost. 2014 Nov;112(5):972-80. doi: 10.1160/TH14-03-0198. Epub 2014 Aug 7.
4
Factor VIII deficiency does not protect against atherosclerosis.VIII 因子缺乏症不能预防动脉粥样硬化。
J Thromb Haemost. 2012 Jan;10(1):30-7. doi: 10.1111/j.1538-7836.2011.04499.x.
5
Atherosclerotic heart disease: prevalence and risk factors in hospitalized men with haemophilia A.动脉粥样硬化性心脏病:住院甲型血友病男性患者的患病率及危险因素。
Haemophilia. 2011 Nov;17(6):867-71. doi: 10.1111/j.1365-2516.2011.02501.x. Epub 2011 Mar 4.
6
Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era.基于凝血、显色和免疫测定的先天性因子 X 缺陷分类的持续有效性,即使在分子生物学时代也是如此。
Haemophilia. 2011 Jan;17(1):17-20. doi: 10.1111/j.1365-2516.2010.02328.x.
7
Prothrombin complex concentrate such as therapy and prophylaxis in factor X-deficient patient (Friuli variant).凝血酶原复合物浓缩物,如因子 X 缺乏症患者(弗留利变异型)的治疗和预防。
Clin Appl Thromb Hemost. 2011 Aug;17(4):332-6. doi: 10.1177/1076029610365331. Epub 2010 Mar 22.
8
Factor X deficiency.凝血因子X缺乏症
Semin Thromb Hemost. 2009 Jun;35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13.
9
The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency.先天性凝血酶原或 FX 缺乏症患者无动脉或静脉血栓形成的临床意义。
J Thromb Thrombolysis. 2010 Apr;29(3):299-302. doi: 10.1007/s11239-009-0342-2.
10
Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: a critical evaluation.仅在外源性或内源性系统中存在缺陷或主要存在缺陷的先天性因子X缺乏症:一项批判性评估。
Am J Hematol. 2008 Aug;83(8):668-71. doi: 10.1002/ajh.21207.

弗留利X因子凝血障碍:近50年后

Factor X Friuli Coagulation Disorder: Almost 50 Years Later.

作者信息

Girolami Antonio, Cosi Elisabetta, Santarossa Claudia, Ferrari Silvia, Girolami Bruno, Lombardi Anna Maria

机构信息

1 Department of Medicine, University of Padua Medical School, Padua, Italy.

2 Division of Medicine, Padua City Hospital, Padua, Italy.

出版信息

Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29.

DOI:10.1177/1076029616686423
PMID:28030967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6714644/
Abstract

The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. However, the story of that disease was an international event since patients with this defect were studied in France and in Italy, and different diagnoses were reached-FVII; FX; combined prothrombin complex; and combined FII, FVII, and FX deficiencies. The diagnostic difficulties were due to the peculiar clotting pattern presented by these patients, namely, prolonged partial thromboplastin time, prolonged prothrombin time but normal Russell viper venom clotting time. Only suitable anti-FX antisera clarified the pattern. Altogether 12 homozygotes and 102 heterozygotes have been followed during 4 decades. Six homozygotes died, 2 of them due to HIV infection and 1 due to hepatitis B liver cirrhosis. The other 3 died of nontransfusion-related morbidity. Bleeding tendency has been moderate in agreement with the extrinsic or intrinsic system assay results-FX level of 4% to 5% is considered normal. Heterozygotes may present occasional bleeding manifestations usually during surgery or delivery. Molecular analysis have shown that the mutation responsible for the defect is a Pro343Ser substitution in exon 8. Chimeric FX Friuli mice have been useful in studying the effect of FX levels on embryonic or natal mortality of these animals. No new homozygote but several heterozygotes have been recently seen. The study of FX Friuli has revolutionized the diagnostic approach to FX deficiencies. The FX should be assayed by all assay systems. The FX Friuli has never been described in any other country, and all patients studied come from the Friuli Meduna River Valley.

摘要

弗留利因子X(FX)的故事。弗留利因子X于1969年至1970年被发现。然而,该疾病的故事是一个国际事件,因为患有这种缺陷的患者在法国和意大利都有研究,并且得出了不同的诊断结果——FVII;FX;凝血酶原复合物联合缺乏;以及FII、FVII和FX联合缺乏。诊断困难是由于这些患者呈现出特殊的凝血模式,即部分凝血活酶时间延长、凝血酶原时间延长但罗素蝰蛇毒凝血时间正常。只有合适的抗FX抗血清才能阐明这种模式。在40年期间共追踪了12名纯合子和102名杂合子。6名纯合子死亡,其中2人死于HIV感染,1人死于乙型肝炎肝硬化。另外3人死于与输血无关的疾病。出血倾向为中度,这与外源性或内源性系统检测结果一致——FX水平为4%至5%被认为是正常的。杂合子可能偶尔出现出血表现,通常在手术或分娩期间。分子分析表明,导致该缺陷的突变是外显子8中的Pro343Ser替代。嵌合弗留利因子X小鼠有助于研究FX水平对这些动物胚胎或出生死亡率的影响。最近没有发现新的纯合子,但发现了几个杂合子。对弗留利因子X的研究彻底改变了FX缺乏症的诊断方法。所有检测系统都应检测FX。弗留利因子X在其他任何国家都未曾被描述过,所有研究的患者都来自弗留利梅杜纳河谷。