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原发性免疫缺陷中的腺苷脱氨酶缺乏症(作者译)

[Adenosine deaminase deficiency in primary immunodeficiencies (author's transl)].

作者信息

Belohradsky B H, Hennig N, Marget W, Fudenberg H H

出版信息

Klin Wochenschr. 1976 Dec 1;54(23):1109-15. doi: 10.1007/BF01469254.

Abstract

The occurrence of severe combined immunodeficiency (SCID) with adenosine deaminase (ADA) deficiency in erythrocytes has been reported in 14 patients. Enzyme deficiency may result in early depression of the lymphatic system. ADA is detectable in different tissues by photometric and electrophoretic methods. The gene locus for ADA has been localised on chromosome 20. Studies on the enzyme defect in different forms of primary immunodeficiencies led to the description of a well defined nosological entity. New aspects can be expected in the fields of pathogenesis, prenatal diagnosis, genetic councelling, and possibly therapeutic trials.

摘要

据报道,14例患者出现了严重联合免疫缺陷(SCID)并伴有红细胞腺苷脱氨酶(ADA)缺乏。酶缺乏可能导致淋巴系统早期抑制。通过光度法和电泳法可在不同组织中检测到ADA。ADA的基因位点已定位在20号染色体上。对不同形式原发性免疫缺陷中酶缺陷的研究导致了一个明确的疾病实体的描述。在发病机制、产前诊断、遗传咨询以及可能的治疗试验等领域有望出现新的进展。

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