• 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

The camptodactyly-arthropathy-pericarditis syndrome: case report and literature review.

作者信息

Laxer R M, Cameron B J, Chaisson D, Smith C R, Stein L D

出版信息

Arthritis Rheum. 1986 Mar;29(3):439-44. doi: 10.1002/art.1780290322.

DOI:10.1002/art.1780290322
PMID:3964321
Abstract
摘要

相似文献

1
The camptodactyly-arthropathy-pericarditis syndrome: case report and literature review.屈曲指-关节病-心包炎综合征：病例报告及文献综述
Arthritis Rheum. 1986 Mar;29(3):439-44. doi: 10.1002/art.1780290322.
2
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy.屈曲指-关节病-髋内翻-心包炎综合征与幼年特发性关节病
AJR Am J Roentgenol. 2005 Aug;185(2):522-9. doi: 10.2214/ajr.185.2.01850522.
3
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.屈曲指-关节病-髋内翻-心包炎综合征：临床特征及基因定位到人类1号染色体
Arthritis Rheum. 1998 Apr;41(4):730-5. doi: 10.1002/1529-0131(199804)41:4<730::AID-ART22>3.0.CO;2-Y.
4
Syndrome of progressive deforming non-inflammatory arthritis of childhood: two patients of camptodactyly-arthropathy-coxa vara-pericarditis syndrome.儿童进行性变形非炎症性关节炎综合征：Camptodactyly-arthropathy-coxa vara-pericarditis 综合征两例
Rheumatol Int. 2021 Oct;41(10):1875-1882. doi: 10.1007/s00296-020-04688-0. Epub 2020 Aug 19.
5
Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: clinical and molecular genetic findings in 22 patients.沙特阿拉伯的指节骨-关节病-髋关节-心包炎综合征：22 例患者的临床和分子遗传学发现。
Semin Arthritis Rheum. 2013 Oct;43(2):292-6. doi: 10.1016/j.semarthrit.2012.11.004. Epub 2013 Jan 2.
6
A familial syndrome of pericarditis, arthritis, and camptodactyly.
N Engl J Med. 1983 Jul 28;309(4):224-5. doi: 10.1056/NEJM198307283090407.
7
The pathology of the involved tendons in patients with familial arthropathy and congenital camptodactyly.
Arthritis Rheum. 1983 Jul;26(7):896-900. doi: 10.1002/art.1780260711.
8
Juvenile rheumatoid arthritis with cardiac tamponade.青少年类风湿关节炎伴心脏压塞
Ann Rheum Dis. 1978 Jun;37(3):273-6. doi: 10.1136/ard.37.3.273.
9
A familial syndrome of pericarditis, arthritis, camptodactyly, and coxa vara.一种伴有心包炎、关节炎、屈曲指及髋内翻的家族性综合征。
Arthritis Rheum. 1986 Mar;29(3):436-8. doi: 10.1002/art.1780290321.
10
Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.屈曲指-关节病-髋内翻-心包炎（CACP）综合征中的蛋白丢失性肠病
Pediatr Rheumatol Online J. 2016 May 25;14(1):32. doi: 10.1186/s12969-016-0093-5.

引用本文的文献

1
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Caused by Truncating Mutations in the Gene: Case Series and Literature Review.由该基因截短突变引起的屈曲指-关节病-髋内翻-心包炎综合征：病例系列及文献综述
Mol Syndromol. 2025 May;16(3):223-234. doi: 10.1159/000542596. Epub 2024 Nov 13.
2
A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.一种新型蛋白聚糖 4 基因突变导致 CACP 综合征：两姐妹报告。
Pediatr Rheumatol Online J. 2023 Jan 24;21(1):8. doi: 10.1186/s12969-023-00793-z.
3
Pseudo-rheumatic manifestations of limping: Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: Single case report and review of the literature.
跛行的假性风湿性表现：屈曲指-关节病-髋内翻-心包炎综合征：病例报告及文献复习
Front Pediatr. 2022 Dec 5;10:981938. doi: 10.3389/fped.2022.981938. eCollection 2022.
4
The Efficacy of Yttrium-90 Radiosynovectomy in Patients with Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome.钇-90放射性滑膜切除术治疗屈曲指-关节病-髋内翻-心包炎综合征患者的疗效
Mol Imaging Radionucl Ther. 2017 Feb 5;26(1):33-37. doi: 10.4274/mirt.29484.
5
Camptodactyly, arthropathy, coxa vara, pericarditis (CACP)syndrome: a case report.屈曲指、关节病、髋内翻、心包炎（CACP）综合征：一例报告
J Korean Med Sci. 2004 Dec;19(6):907-10. doi: 10.3346/jkms.2004.19.6.907.
6
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16.家族性肉芽肿性炎性关节炎、皮疹和葡萄膜炎与16号染色体的遗传连锁。
Am J Hum Genet. 1996 Nov;59(5):1097-107.