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遗传性CD4 + T淋巴细胞减少症。

Hereditary CD4+ T lymphocytopenia.

作者信息

Freier S, Kerem E, Dranitzki Z, Schlesinger M, Rabinowitz R, Brautbar C, Ashkirat M, Naparstek Y

机构信息

Department of Pediatrics, Shaare Zedek Medical Center, Jerusalem, Israel.

出版信息

Arch Dis Child. 1998 Apr;78(4):371-2. doi: 10.1136/adc.78.4.371.

DOI:10.1136/adc.78.4.371
PMID:9623404
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1717546/
Abstract

Two siblings suffering from mental retardation, progressive bronchiectasis, extensive warts, and persistent hepatitis B are described. The propositus also had an unusual physiognomy and non-specific colitis. Both patients had a marked decrease in the population of CD4+ helper T cells.

摘要

描述了两名患有智力发育迟缓、进行性支气管扩张、广泛疣和持续性乙型肝炎的兄弟姐妹。先证者还具有异常面容和非特异性结肠炎。两名患者的CD4 +辅助性T细胞数量均显著减少。

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本文引用的文献

1
B non-Hodgkin's lymphoma in a haemophilia patient with idiopathic CD4+ T-lymphocytopenia.
Leuk Lymphoma. 1996 Mar;21(1-2):177-80. doi: 10.3109/10428199609067597.
2
NIH conference. New insights into common variable immunodeficiency.美国国立卫生研究院会议。常见变异型免疫缺陷的新见解。
Ann Intern Med. 1993 May 1;118(9):720-30. doi: 10.7326/0003-4819-118-9-199305010-00011.
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Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.主要组织相容性复合体II类缺陷:临床表现、免疫学特征及预后
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CD4+ T lymphocytopenia in children: lack of evidence for a new acquired immunodeficiency syndrome agent.儿童CD4+ T淋巴细胞减少症:缺乏新的获得性免疫缺陷综合征病原体的证据。
Pediatr Infect Dis J. 1995 Jun;14(6):527-35.
5
Unusual phenotypes of human inducer T cells as measured by OKT4 and related monoclonal antibodies.通过OKT4及相关单克隆抗体检测的人类诱导性T细胞的异常表型。
J Immunol. 1981 Sep;127(3):980-2.