• 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

Combined deficiencies of Factor VIII (AHF) and Factor XI (PTA).

作者信息

Lian E C, Deykin D, Harkness D R

出版信息

Am J Hematol. 1976;1(3):319-24. doi: 10.1002/ajh.2830010306.

DOI:10.1002/ajh.2830010306
PMID:998619
Abstract

Combined deficiencies of Factor VIII and Factor XI associated with moderate degree of bleeding symptoms were found in 3 brothers. Examination of Factor VIII activity and Factor VIII-related antigen revealed that the Factor VIII activity/Factor VIII-related antigen ratio was significantly decreased in their mother and maternal grandmother consistent with the carrier state of hemophilia. Factor XI deficiency was found in 2 siblings, the father, and 2 of his sisters. The paternal grandmother was thought to carry the abnormal Factor X I gene, although her Factor XI level was normal, because of a significant bleeding history. It was concluded that the combined Factor VIII and XI deficiencies in the 3 brothers represent the coincidental inheritance of 2 separate and independent abnormal genes.

摘要

相似文献

1
Combined deficiencies of Factor VIII (AHF) and Factor XI (PTA).
Am J Hematol. 1976;1(3):319-24. doi: 10.1002/ajh.2830010306.
2
Familial multiple coagulation factor deficiencies. II. Combined factor VIII, IX, and XI deficiency and combined factor IX and XI deficiency: two previously uncharacterized familial multiple factor deficiency syndromes.家族性多种凝血因子缺乏症。II. 因子VIII、IX和XI联合缺乏症以及因子IX和XI联合缺乏症:两种此前未被描述的家族性多因子缺乏综合征。
Semin Thromb Hemost. 1981 Fall;7(2):149-69. doi: 10.1055/s-2007-1005074.
3
Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi Jews.
Blood Coagul Fibrinolysis. 1994 Feb;5(1):59-62. doi: 10.1097/00001721-199402000-00009.
4
Combined factor VIII and factor XI congenital deficiency: a case report.
Haematologica. 1990 May-Jun;75(3):272-3.
5
Familial multiple coagulation factor deficiencies. I. Review of the literature: Differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states.家族性多种凝血因子缺乏症。I. 文献综述:与多种因子缺乏相关的单一遗传性疾病与单一因子缺乏状态偶然并发的鉴别。
Semin Thromb Hemost. 1981 Fall;7(2):112-48. doi: 10.1055/s-2007-1005073.
6
Combined congenital deficiency of factor V and factor VIII. Report of a further case with some considerations on the hetereditary transmission of this disorder.联合先天性因子V和因子VIII缺乏症。另一例报告及关于该疾病遗传传递的一些思考。
Acta Haematol. 1976;55(4):234-43. doi: 10.1159/000208020.
7
Carriers with excessively low factor VIII procoagulant activity (VIII AHF): a study of two unrelated families with mild hemophilia A.
Blood. 1977 Apr;49(4):607-18.
8
Hereditary plasma thromboplastin antecedent (PTA, FXI) deficiency in a Saudi family.沙特一个家族中的遗传性血浆凝血活酶前体(PTA,FXI)缺乏症。
Clin Lab Haematol. 1988;10(3):307-14. doi: 10.1111/j.1365-2257.1988.tb00024.x.
9
A female hemophilia A combined with hereditary coagulation factor XII deficiency: a case report.一例女性甲型血友病合并遗传性凝血因子Ⅻ缺乏症:病例报告
Am J Hematol. 1992 Feb;39(2):137-41. doi: 10.1002/ajh.2830390212.
10
Definition of the bleeding tendency in factor XI-deficient kindreds--a clinical and laboratory study.XI因子缺乏家族中出血倾向的定义——一项临床与实验室研究
Thromb Haemost. 1995 Feb;73(2):194-202.

引用本文的文献

1
Hemophilia A and C in a female: The first case report in literature.女性血友病A和C:文献中的首例病例报告。
Ann Med Surg (Lond). 2021 Jul 15;68:102561. doi: 10.1016/j.amsu.2021.102561. eCollection 2021 Aug.
2
Congenital Combined Bleeding Disorders, a Comprehensive Study of a Large Number of Iranian Patients.先天性联合出血性疾病:对大量伊朗患者的综合研究。
Clin Appl Thromb Hemost. 2021 Jan-Dec;27:1076029621996813. doi: 10.1177/1076029621996813.