Suppr超能文献

一名患有共济失调-毛细血管扩张症的六岁女孩出现罕见的无神经系统症状情况。

Unusual absence of neurologic symptoms in a six-year old girl with ataxia-telangiectasia.

作者信息

Trimis G G, Athanassaki C K, Kanariou M M, Giannoulia-Karantana A A

机构信息

Pediatric Department of University of Athens, Greece.

出版信息

J Postgrad Med. 2004 Oct-Dec;50(4):270-1.

Abstract

Ataxia-telangiectasia (A-T) is a rare multisystem, neurodegenerative genetic disorder. We present a case of a 6-year-old girl who had a history of frequent respiratory infections and also had ocular and immunological features of this syndrome. The absence of neurological symptoms, which is very unusual for a patient of this age, raised many difficulties in the diagnosis of the disease. It is concluded that a normal neurological assessment must not exclude the diagnosis of A-T and delay the proper interventional measures.

摘要

共济失调毛细血管扩张症(A-T)是一种罕见的多系统神经退行性遗传疾病。我们报告一例6岁女孩,她有频繁呼吸道感染病史,且具有该综合征的眼部和免疫学特征。该年龄患者无神经症状这一情况非常罕见,给疾病诊断带来诸多困难。得出的结论是,正常的神经学评估不能排除A-T的诊断,也不应延迟适当的干预措施。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验