一名患有完全性C2缺乏且NK细胞功能降低的患者反复出现感染、心包炎和肾病，符合急性风湿热和系统性红斑狼疮。 - Suppr

Suppr

超能文献

Recurrent infections, pericarditis and renal disease in a patient with total C2 deficiency and decreased NK cell function consistent with acute rheumatic fever and systemic lupus erythematosus.

作者信息

Bittleman D B, Maves K K, Bertolatus J A, Bonsib S M, Densen P, Ballas Z K, Weiler J M

出版信息

Ann Rheum Dis. 1994 Apr;53(4):280-1. doi: 10.1136/ard.53.4.280.

DOI:10.1136/ard.53.4.280

PMID:8203960

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1005310/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910c/1005310/b2cd8b499ae5/annrheumd00492-0066-a.jpg

相似文献

Recurrent infections, pericarditis and renal disease in a patient with total C2 deficiency and decreased NK cell function consistent with acute rheumatic fever and systemic lupus erythematosus.一名患有完全性C2缺乏且NK细胞功能降低的患者反复出现感染、心包炎和肾病，符合急性风湿热和系统性红斑狼疮。

Ann Rheum Dis. 1994 Apr;53(4):280-1. doi: 10.1136/ard.53.4.280.

[Congenital complement 2 deficiency in a patient with systemic lupus erythematosus with a severe course].[一名患有严重系统性红斑狼疮患者的先天性补体2缺乏症]

Pol Tyg Lek. 1987 Jul 27;42(30):921-3.

Hereditary C2 deficiency and systemic lupus erythematosus associated with severe glomerulonephritis.遗传性C2缺乏症与伴有严重肾小球肾炎的系统性红斑狼疮。

Clin Exp Immunol. 1978 Feb;31(2):328-38.

Lymphocyte transformation with streptolysin S preparations and inhibition of streptolysin S by serum in rheumatic fever and other rheumatic diseases.风湿热及其他风湿性疾病中链球菌溶血素S制剂诱导的淋巴细胞转化及血清对链球菌溶血素S的抑制作用

J Lab Clin Med. 1972 Aug;80(2):165-78.

Association of systemic lupus erythematosus and SLE-like syndromes with hereditary and acquired complement deficiency states.系统性红斑狼疮及类系统性红斑狼疮综合征与遗传性和获得性补体缺乏状态的关联。

Arthritis Rheum. 1978 Jun;21(5 Suppl):S146-52.

Vasculitis with probable familial C2 deficiency. (Case 1). Systemic lupus erythematosus with familial C2 deficiency. (Case 2).可能存在家族性C2缺乏的血管炎。（病例1）。伴有家族性C2缺乏的系统性红斑狼疮。（病例2）。

Proc R Soc Med. 1977 Oct;70(10):733-4. doi: 10.1177/003591577707001021.

Activity of the reticuloendothelial system in diseases of altered immunity.

J Lab Clin Med. 1965 Dec;66(6):952-60.

Homozygous C2 deficiency, lupus erythematosus, and anti-Ro (SSA) antibodies.纯合子C2缺乏、红斑狼疮和抗Ro（SSA）抗体。

Arthritis Rheum. 1983 Oct;26(10):1279-82. doi: 10.1002/art.1780261017.

Properdin levels in systemic lupus erythematosus and membranoproleferative glomerulonephritis.系统性红斑狼疮和膜增生性肾小球肾炎中的备解素水平。

Clin Exp Immunol. 1974 Apr;16(4):575-81.

[Hereditary C2 deficiency with systemic lupus erythematosus: clinical and immunologic studies in a family (author's transl)].

Nouv Presse Med. 1977 Oct 22;6(35):3199-203.

引用本文的文献

Natural killer cell dysfunction during acute infection with foot-and-mouth disease virus.口蹄疫病毒急性感染期间自然杀伤细胞功能障碍

Clin Vaccine Immunol. 2009 Dec;16(12):1738-49. doi: 10.1128/CVI.00280-09. Epub 2009 Oct 14.

本文引用的文献

Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency.补体缺陷状态与感染：免疫缺陷状态下奈瑟菌及其他感染的流行病学、发病机制及后果

Medicine (Baltimore). 1984 Sep;63(5):243-73.

C2 deficiency. Development of lupus erythematosus.C2缺乏。红斑狼疮的发展。

J Clin Invest. 1973 Jul;52(7):1601-7. doi: 10.1172/JCI107337.

Lupus diseases associated with hereditary and acquired deficiencies of complement.与遗传性和获得性补体缺陷相关的狼疮疾病。

Springer Semin Immunopathol. 1986;9(2-3):161-78. doi: 10.1007/BF02099020.

Infectious diseases associated with complement deficiencies.与补体缺陷相关的传染病。

Clin Microbiol Rev. 1991 Jul;4(3):359-95. doi: 10.1128/CMR.4.3.359.

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing.I型人类补体C2缺陷。一个28个碱基对的基因缺失导致RNA剪接过程中外显子6的跳跃。

J Biol Chem. 1992 May 5;267(13):9347-53.

Molecular heterogeneity of C2 deficiency.C2缺陷的分子异质性

N Engl J Med. 1992 Mar 26;326(13):871-4. doi: 10.1056/NEJM199203263261306.

Proc R Soc Med. 1977 Oct;70(10):733-4. doi: 10.1177/003591577707001021.

Hereditary C2 deficiency and systemic lupus erythematosus associated with severe glomerulonephritis.遗传性C2缺乏症与伴有严重肾小球肾炎的系统性红斑狼疮。

Clin Exp Immunol. 1978 Feb;31(2):328-38.

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