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共济失调毛细血管扩张症在同一家族中的不同临床和免疫学表现。

Different clinical and immunological presentation of ataxia-telangiectasia within the same family.

作者信息

Soresina A, Meini A, Lougaris V, Cattaneo G, Pellegrino S, Piane M, Darra F, Plebani A

机构信息

1Department of Pediatrics and Institute of Molecular Medicine A. Nocivelli, University of Brescia, Brescia, Italy.

出版信息

Neuropediatrics. 2008 Feb;39(1):43-5. doi: 10.1055/s-2008-1076736.

Abstract

Ataxia-telangiectasia is a rare multisystem neurodegenerative genetic disorder due to mutation of ATM gene. The clinical expression and the immunological abnormalities are variable and apparently not associated with the type of ATM mutations. We report on two siblings affected by A-T with different clinical and immunological presentations; in particular in one the immunological phenotype was reminiscent of hyper IgM syndrome.

摘要

共济失调毛细血管扩张症是一种罕见的多系统神经退行性遗传疾病,由ATM基因突变引起。其临床表现和免疫异常具有多样性,且显然与ATM突变类型无关。我们报告了两名患有共济失调毛细血管扩张症的兄弟姐妹,他们具有不同的临床和免疫表现;特别是其中一人的免疫表型让人联想到高IgM综合征。

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