• 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

儿童免疫缺陷的诊断。

Diagnosis of immunologic deficiency in childhood.

作者信息

Edelson P J

出版信息

Calif Med. 1972 Apr;116(4):19-24.

PMID:5019089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1518345/
Abstract

A defective host response may be responsible for recurring infections in certain children. Recognition of these defects may be important both therapeutically for the patient and for genetic counseling for the family. Family history, age of onset of illness and type of infecting agents may all point to one or another defect in host resistance. An initial evaluation for suspected immunologic disease may be rapidly accomplished and should include absolute neutrophil and lymphocyte counts, chest X-ray for a thymic shadow, Schick test for functional IgG antibodies and isohemagglutinin titers for functional IgM antibodies. Although serum protein electrophoresis is unreliable for diagnosis of most disorders of circulating antibodies, quantitation of the IgG, IgA and IgM antibody classes is generally available. More extensive studies may be carried out to further define defects in the cell-mediated immune system, in the various complement components, or in the ingestion and killing of bacteria by neutrophils.

摘要

宿主反应缺陷可能是某些儿童反复感染的原因。识别这些缺陷对于患者的治疗以及家庭的遗传咨询都可能很重要。家族史、发病年龄和感染病原体类型都可能指向宿主抵抗力的一种或另一种缺陷。对疑似免疫疾病的初步评估可以迅速完成,应包括绝对中性粒细胞和淋巴细胞计数、胸部X光检查胸腺阴影、检测功能性IgG抗体的锡克试验以及检测功能性IgM抗体的同种血凝素滴度。虽然血清蛋白电泳对于大多数循环抗体疾病的诊断不可靠,但通常可以对IgG、IgA和IgM抗体类别进行定量。可以进行更广泛的研究以进一步确定细胞介导免疫系统、各种补体成分或中性粒细胞对细菌的吞噬和杀伤方面的缺陷。

相似文献

1
Diagnosis of immunologic deficiency in childhood.儿童免疫缺陷的诊断。
Calif Med. 1972 Apr;116(4):19-24.
2
Immune deficiency disease of undetermined aetiology in infancy.婴儿期病因不明的免疫缺陷病。
S Afr Med J. 1974 Apr 6;48(16):687-90.
3
[Antibody deficiency without decrease in the level of serum immunoglobulins].血清免疫球蛋白水平未降低的抗体缺乏症
Arch Fr Pediatr. 1984 Dec;41(10):673-9.
4
[Diagnosis and treatment of primary antibody deficiency syndromes].[原发性抗体缺陷综合征的诊断与治疗]
Ugeskr Laeger. 2018 Feb 26;180(9).
5
When to think of immunodeficiency?何时考虑免疫缺陷?
Adv Exp Med Biol. 2013;764:167-77. doi: 10.1007/978-1-4614-4726-9_14.
6
Laboratory screening for the diagnosis of children with primary immunodeficiencies.
J Investig Allergol Clin Immunol. 1991 Jun;1(3):195-200.
7
[Laboratory diagnosis of immune deficiency].[免疫缺陷的实验室诊断]
Infusionsther Transfusionsmed. 1993 Apr;20 Suppl 1:56-67.
8
The Schick test. A useful tool for screening for antibody deficiency.锡克试验。一种用于筛查抗体缺乏的有用工具。
Am J Dis Child. 1981 Jul;135(7):618-20.
9
Anti-capsular polysaccharide antibody deficiency states.抗荚膜多糖抗体缺乏状态。
Immunodeficiency. 1993;5(1):1-21.
10
[Laboratory diagnosis of immunoglobulin deficiencies].[免疫球蛋白缺乏症的实验室诊断]
Postepy Hig Med Dosw. 2002;56 Suppl:13-21.

本文引用的文献

1
Agammaglobulinemia.无丙种球蛋白血症
Pediatrics. 1952 Jun;9(6):722-8.
2
THE PATHOGENESIS OF IMMUNOLOGIC DEFICIENCY DISEASES.免疫缺陷病的发病机制。
Am J Med. 1965 Apr;38:579-604. doi: 10.1016/0002-9343(65)90135-x.
3
Phytohaemagglutinin unresponsiveness of lymphocytes from babies with congenital rubella.先天性风疹患儿淋巴细胞对植物血凝素的无反应性
Nature. 1967 May 13;214(5089):695-6. doi: 10.1038/214695a0.
4
In vitro bactericidal capacity of human polymorphonuclear leukocytes: diminished activity in chronic granulomatous disease of childhood.人多形核白细胞的体外杀菌能力:儿童慢性肉芽肿病中活性降低。
J Clin Invest. 1967 Apr;46(4):668-79. doi: 10.1172/JCI105568.
5
Chediak-Higashi syndrome: hereditary gigantism of cytoplasmic organelles.
Science. 1966 Jan 7;151(3706):81-3. doi: 10.1126/science.151.3706.81.
6
Hereditary lymphopenic agammaglobulinemia associated with a distinctive form of short-limbed dwarfism and ectodermal dysplasia.遗传性淋巴细胞减少性无丙种球蛋白血症,伴有一种特殊类型的短肢侏儒症和外胚层发育不良。
J Pediatr. 1969 Oct;75(4):675-84. doi: 10.1016/s0022-3476(69)80465-8.
7
Thymic dysplasia. A separable entity from "swiss agammaglobulinemia".胸腺发育不全。一种与“瑞士型无丙种球蛋白血症”可区分的病症。
Am J Med Sci. 1967 Jun;253(6):741-50. doi: 10.1097/00000441-196706000-00012.
8
Wiskott-Aldrich syndrome, a genetically determined cellular immunologic deficiency: clinical and laboratory responses to therapy with transfer factor.威斯科特-奥尔德里奇综合征,一种由基因决定的细胞免疫缺陷病:对转移因子治疗的临床及实验室反应
Proc Natl Acad Sci U S A. 1970 Oct;67(2):821-8. doi: 10.1073/pnas.67.2.821.
9
Analytic review: disorders of phagocyte function.分析性综述:吞噬细胞功能障碍
Blood. 1970 Jun;35(6):851-66.