• 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

在一个荷兰家族中,遗传性补体第三成分缺乏与复发性化脓性感染、循环免疫复合物及血管炎相关。

Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family.

作者信息

Roord J J, Daha M, Kuis W, Verbrugh H A, Verhoef J, Zegers B J, Stoop J W

出版信息

Pediatrics. 1983 Jan;71(1):81-7.

PMID:6848983
Abstract

A family is described in which 3/11 children showed a homozygous deficiency of C3, and both parents and six other children had subnormal levels of C3. The three children with selective C3 deficiency suffered repeatedly from bacterial infections, whereas the parents and the other siblings were clinically healthy. During infectious episodes the patients showed a maculopapular skin rash, and at such times immune complexes were present in the serum. Biopsy specimens of the skin lesions showed the picture of leukocytoclastic vasculitis.

摘要

报道了一个家庭,其中11个孩子中有3个表现出C3纯合缺陷,父母和其他6个孩子的C3水平低于正常。3名患有选择性C3缺陷的儿童反复遭受细菌感染,而父母和其他兄弟姐妹临床健康。在感染发作期间,患者出现斑丘疹性皮疹,此时血清中存在免疫复合物。皮肤病变的活检标本显示白细胞破碎性血管炎的表现。

相似文献

1
Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family.在一个荷兰家族中,遗传性补体第三成分缺乏与复发性化脓性感染、循环免疫复合物及血管炎相关。
Pediatrics. 1983 Jan;71(1):81-7.
2
[Barraquer and Simons lipodystrophy. Complement anomalies and cutaneous leukocytoclasic vasculitis].[巴拉奎尔和西蒙斯脂肪营养不良。补体异常与皮肤白细胞破碎性血管炎]
Ann Dermatol Venereol. 1987;114(9):1083-91.
3
Inherited C3 deficiency with recurrent infections and glomerulonephritis.伴有反复感染和肾小球肾炎的遗传性C3缺乏症。
Am J Dis Child. 1988 Jan;142(1):79-83. doi: 10.1001/archpedi.1988.02150010089032.
4
Demonstration of circulating and tissue-fixed immune complexes in cutaneous necrotizing vasculitis.皮肤坏死性血管炎中循环免疫复合物和组织固定免疫复合物的证实。
Acta Derm Venereol. 1980;60(5):389-92.
5
Hereditary complement factor I deficiency.
QJM. 1994 Jul;87(7):385-401.
6
Membrane attack complex of complement in leukocytoclastic vasculitis of the skin. Presence and possible pathogenetic role.补体膜攻击复合物在皮肤白细胞破碎性血管炎中的作用。其存在情况及可能的致病机制
Arch Dermatol. 1987 Sep;123(9):1192-5.
7
Acute generalized pustular bacterid and immune complexes.
Acta Derm Venereol. 1980;60(1):66-9.
8
[Sequential analysis of immune complexes in vasculitis].
Rev Clin Esp. 1984 Sep 15;174(5):153-7.
9
Complement factor I deficiency with recurrent aseptic meningitis.伴有复发性无菌性脑膜炎的补体因子I缺乏症
Arch Intern Med. 1993 Jun 14;153(11):1380-3.
10
Immune complexes in the reactive inflammatory vascular dermatoses.反应性炎症性血管性皮肤病中的免疫复合物。
Dermatol Clin. 1985 Jan;3(1):185-90.

引用本文的文献

1
The complement system and human autoimmune diseases.补体系统与人类自身免疫性疾病。
J Autoimmun. 2023 May;137:102979. doi: 10.1016/j.jaut.2022.102979. Epub 2022 Dec 18.
2
Homozygous hereditary C3 deficiency due to a premature stop codon.由于过早终止密码子导致的纯合子遗传性C3缺乏症。
J Clin Immunol. 2002 Nov;22(6):321-30. doi: 10.1023/a:1020665614139.
3
Functional deficiency of complement factor D in a monozygous twin.单卵双胞胎中补体因子D的功能缺陷
Clin Exp Immunol. 1984 Dec;58(3):724-30.
4
Structure and expression of the C3 gene.补体C3基因的结构与表达
Springer Semin Immunopathol. 1983;6(2-3):119-47. doi: 10.1007/BF00205869.
5
Analysis of C3-receptor activity on human B-lymphocytes and isolation of the complement receptor type 2 (CR2).人B淋巴细胞上C3受体活性分析及2型补体受体(CR2)的分离
Biochem J. 1984 Nov 15;224(1):75-86. doi: 10.1042/bj2240075.
6
Surface hydrophobicity and opsonic requirements of coagulase-negative staphylococci in suspension and adhering to a polymer substratum.凝固酶阴性葡萄球菌在悬浮状态及附着于聚合物基质时的表面疏水性及调理素需求
Eur J Clin Microbiol Infect Dis. 1988 Apr;7(2):161-6. doi: 10.1007/BF01963070.
7
Loss of complement receptor type 1 (CR1) on ageing of erythrocytes. Studies of proteolytic release of the receptor.红细胞衰老过程中补体受体1(CR1)的丧失。受体蛋白水解释放的研究。
Biochem J. 1986 May 1;235(3):815-21. doi: 10.1042/bj2350815.
8
Human complement component C3: cDNA coding sequence and derived primary structure.人补体成分C3:cDNA编码序列及推导的一级结构。
Proc Natl Acad Sci U S A. 1985 Feb;82(3):708-12. doi: 10.1073/pnas.82.3.708.
9
Molecular basis of hereditary C3 deficiency.遗传性C3缺乏症的分子基础。
J Clin Invest. 1990 Oct;86(4):1158-63. doi: 10.1172/JCI114821.
10
The inaccessibility of the outer membrane of adherent Treponema pallidum (Nichols strain) to anti-treponemal antibodies, a possible role of serum proteins.梅毒螺旋体(Nichols株)外膜对抗梅毒螺旋体抗体不可及,血清蛋白的可能作用。
Genitourin Med. 1990 Jun;66(3):165-70. doi: 10.1136/sti.66.3.165.