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遗传性重症联合免疫缺陷症和腺苷脱氨酶缺乏症

Hereditary sever combined immunodeficiency and adenosine deaminase deficiency.

作者信息

Ackeret C, Llüss H J, Hitzig W H

出版信息

Pediatr Res. 1976 Jan;10(1):67-70. doi: 10.1203/00006450-197601000-00013.

Abstract

A retrospective study aiming at detection of heterozygous carriers of blood adenosine deaminase (ADA) deficiency was carried out in nine families known to us because children had died of combined immunodeficiency (SCID). The trait was found in 3 of 9 parent couples, and in 14 other relatives. In two families one homozygous patient was identified. A total of 54 family members and 60 healthy control subjects were tested. Clinically, the patients were all characterized by marked lymphopenia, nearly normal immunoglobulin levels, and inability to produce antibodies. One homozygous patient recovered after transplantation of fetal liver and thymus and is immunologically normal 1.5 years afterwards.

摘要

我们针对9个家庭开展了一项回顾性研究,这些家庭为我们所知是因为其孩子死于联合免疫缺陷病(SCID),研究目的是检测血液腺苷脱氨酶(ADA)缺乏的杂合子携带者。在9对父母中,有3对发现携带该性状,另外在14名其他亲属中也有发现。在两个家庭中,各鉴定出1名纯合子患者。总共对54名家庭成员和60名健康对照者进行了检测。临床上,这些患者的共同特征是明显的淋巴细胞减少、免疫球蛋白水平几乎正常以及无法产生抗体。1名纯合子患者在接受胎儿肝脏和胸腺移植后康复,1.5年后免疫功能正常。

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