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不常见血清群引起的脑膜炎球菌病患者的耳聋、补体缺陷及免疫球蛋白状态

Deafness, complement deficiencies and immunoglobulin status in patients with meningococcal diseases due to uncommon serogroups.

作者信息

Mayatepek E, Grauer M, Hänsch G M, Sonntag H G

机构信息

University Children's Hospital, Heidelberg, Germany.

出版信息

Pediatr Infect Dis J. 1993 Oct;12(10):808-11. doi: 10.1097/00006454-199310000-00002.

Abstract

The prevalence of deafness and complement deficiencies in association with meningococcal disease caused by uncommon serogroups of meningococci was studied in 30 patients (Group A) and 30 controls with Serogroup B disease (Group B). In Group A 8 patients (26.6%) had hearing impairment in contrast to only 1 patient (3.3%) in Group B (P < 0.01). Complement deficiency was detected in 8 patients (26.6%) of Group A whereas none of the Group B patients showed a defect in the complement system (P < 0.01). Association between complement deficiencies and meningococcal disease was detected for Serogroups Y (n = 5; 16.6%) and W135 (n = 3; 10.0%). Localization of the defects revealed only complement deficiencies of the classical pathway (C8-beta or C7 defects). The levels of Ig and IgG subclasses were found to be within the normal range for all patients. Our results suggest that meningococcal diseases caused by uncommon serogroups are more often associated with deafness and late complement component defects.

摘要

对30例由不常见血清群脑膜炎球菌引起的脑膜炎球菌病患者(A组)和30例B群脑膜炎球菌病对照患者(B组),研究了耳聋及补体缺陷与脑膜炎球菌病的相关性。A组有8例患者(26.6%)有听力障碍,而B组只有1例患者(3.3%)有听力障碍(P<0.01)。A组8例患者(26.6%)检测到补体缺陷,而B组患者均未显示补体系统缺陷(P<0.01)。在Y群(n=5;16.6%)和W135群(n=3;10.0%)中检测到补体缺陷与脑膜炎球菌病之间的关联。缺陷定位显示仅经典途径的补体缺陷(C8-β或C7缺陷)。所有患者的Ig和IgG亚类水平均在正常范围内。我们的结果表明,由不常见血清群引起的脑膜炎球菌病更常与耳聋和晚期补体成分缺陷相关。

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