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与一种罕见的免疫球蛋白异常血症相关的慢性肺部疾病。

Chronic pulmonary disease associated with an unusual dysgammaglobulinaemia.

作者信息

Tennenbaum J I, St Pierre R L, Cerilli G J

出版信息

Clin Exp Immunol. 1968 Nov;3(9):983-8.

Abstract

A 26-year-old patient, subject to recurrent sino-pulmonary infections, with a previously unreported combination of immunological deficiencies is reported. There was a lack of serum immunoglobulin A, salivary immunoglobulin A, decreased serum immunoglobulin M and a deficiency of cellular immunity. It is suggested that this combination of deficits may represent a of hereditary ataxia telangiectasia.

摘要

报告了一名26岁的患者,该患者反复发生鼻窦肺部感染,存在一种先前未报道的免疫缺陷组合。血清免疫球蛋白A、唾液免疫球蛋白A缺乏,血清免疫球蛋白M降低,细胞免疫功能缺陷。提示这种缺陷组合可能代表一种遗传性共济失调毛细血管扩张症。

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本文引用的文献

1
Agammaglobulinemia.无丙种球蛋白血症
Pediatrics. 1952 Jun;9(6):722-8.
5
QUALITATIVE AND QUANTITATIVE IMMUNOGLOBULIN DEFICIENCY.定性和定量免疫球蛋白缺乏症
Am J Med. 1964 Oct;37:602-9. doi: 10.1016/0002-9343(64)90072-5.
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[Clinical aspects of the antibody deficiency syndrome].
Helv Med Acta. 1959 May;26(2):163-202 contd.
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Gamma-A deficiency and hypochromic anemia due to defective iron mobilization.
N Engl J Med. 1967 Apr 20;276(16):886-94. doi: 10.1056/NEJM196704202761602.
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Cellular reactivity to Candida albicans antigen.细胞对白色念珠菌抗原的反应性。
N Engl J Med. 1966 Sep 29;275(13):690-3. doi: 10.1056/NEJM196609292751302.

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