Suppr超能文献

疑似眼组织胞浆菌病黄斑病变中的HLA - B7

HLA-B7 in presumed ocular histoplasmosis maculopathy.

作者信息

Godfrey W A, Cross D E, Ziemianski M C, Sabates R

出版信息

Transplant Proc. 1979 Dec;11(4):1874-6.

PMID:531932
Abstract

Sixty-four patients that fulfill the clinical criteria of the presumed ocular histoplasmosis syndrome were typed for common histocompatibility antigens. The clinical criteria included the presence of multiple peripheral punched out choroidal atropic scars, a clear vitreous, and compatible macular disciform lesions in at least one eye. Thirty-four patients were found to have HLA-B7, which is statistically significant at the p less than 0.005 level when compared to a normal population. Though this is statistically significant, other factors must be involved, as there still remain many patients with this clinical picture who do not demonstrate a common histocompatibility antigen.

摘要

对64例符合疑似眼组织胞浆菌病综合征临床标准的患者进行了常见组织相容性抗原分型。临床标准包括至少一只眼存在多个周边凿孔状脉络膜萎缩性瘢痕、玻璃体清晰以及符合条件的黄斑盘状病变。发现34例患者具有HLA - B7,与正常人群相比,在p小于0.005水平具有统计学意义。尽管这具有统计学意义,但必然还涉及其他因素,因为仍有许多具有此临床症状的患者未表现出共同的组织相容性抗原。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验