• 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

[Bernard-Soulier syndrome in a Swiss family].

作者信息

de Moerloose P, Vogel J J, Clemetson K J, Petite J, Bienz D, Bouvier C A

机构信息

Unité d'hémostase, Hôpital cantonal universitaire, Genève.

出版信息

Schweiz Med Wochenschr. 1987 Nov 14;117(46):1817-21.

PMID:3423769
Abstract

We report the case of a 38-year-old woman with hemorrhagic diathesis. Since early childhood she has suffered from epistaxis, gingival bleeding, ecchymoses and, since puberty, very frequent menorrhagia. Prolongation of bleeding time and thrombocytopenia (100,000 platelets/microliter) with giant platelets were observed. Since idiopathic thrombopenic purpura was suspected, splenectomy was performed. Neither this nor steroid treatment caused any improvement. The patient was able to give birth to an unaffected child, but delivery was followed by a major hemorrhage. In 1986, hysterectomy was considered because of frequent menorrhagia and, therefore, the patient's hemostasis was reinvestigated. The aforementioned abnormalities were confirmed and complementary examinations by electron microscope revealed giant platelets without granular abnormalities. While von Willebrand factor was normal, ristocetin agglutination was defective and analysis of platelet membrane glycoproteins showed absence of glycoprotein Ib. - These observations prompted the diagnosis of Bernard-Soulier syndrome. The study of the family demonstrated that 6 family members were heterozygote. This is believed to be the first large Bernard-Soulier family reported in Switzerland.

摘要

相似文献

1
[Bernard-Soulier syndrome in a Swiss family].
Schweiz Med Wochenschr. 1987 Nov 14;117(46):1817-21.
2
Bernard-Soulier syndrome in a Turkish family.一个土耳其家庭中的伯纳德-索利尔综合征
Int J Clin Pract. 2002 Sep;56(7):546-8.
3
Bernard-Soulier syndrome: a new platelet glycoprotein abnormality. Its relationship with platelet adhesion to subendothelium and with the factor VIII von Willebrand protein.伯纳德-索利尔综合征:一种新的血小板糖蛋白异常。它与血小板黏附于内皮下以及与因子VIII血管性血友病蛋白的关系。
J Lab Clin Med. 1976 Apr;87(4):586-96.
4
Bernard-Soulier syndrome: a case report.
Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:219-21.
5
[Bernard-Soulier syndrome. An important differential diagnosis in chronic thrombocytopenia with bleeding complications].[伯纳德-索利尔综合征。慢性血小板减少伴出血并发症的重要鉴别诊断]
Monatsschr Kinderheilkd. 1993 Jun;141(6):483-6.
6
Molecular defects of platelets in Bernard-Soulier syndrome.伯纳德-索利尔综合征中血小板的分子缺陷
Blood Cells. 1983;9(2):333-58.
7
A large Swiss family with Bernard-Soulier syndrome - Correlation phenotype and genotype.一个患有伯纳德-索利尔综合征的瑞士大家庭——表型与基因型的相关性
Hamostaseologie. 2009 May;29(2):161-7.
8
Role of platelet membrane glycoproteins Ib/IX and IIb/IIIa, and of platelet alpha-granule proteins in platelet aggregation induced by human osteosarcoma cells.血小板膜糖蛋白Ib/IX和IIb/IIIa以及血小板α-颗粒蛋白在人骨肉瘤细胞诱导的血小板聚集中的作用
Cancer Res. 1993 Oct 1;53(19):4695-700.
9
The defective prothrombin consumption in Bernard-Soulier syndrome. Hypotheses from 1948 to 1982.
Blood Cells. 1983;9(2):389-99.
10
Bernard-Soulier syndrome with severe bleeding: absent platelet glycoprotein Ib alpha due to a homozygous one-base deletion.伴有严重出血的伯纳德-索利尔综合征:由于纯合单碱基缺失导致血小板糖蛋白 Ibα 缺失。
Thromb Haemost. 1996 Nov;76(5):670-4.

引用本文的文献

1
Bernard-Soulier syndrome or idiopathic thrombocytopenic purpura: A case series.伯纳德-索利尔综合征或特发性血小板减少性紫癜:病例系列
Caspian J Intern Med. 2020 Winter;11(1):105-109. doi: 10.22088/cjim.11.1.105.