Trimis G G, Athanassaki C K, Kanariou M M, Giannoulia-Karantana A A
Pediatric Department of University of Athens, Greece.
J Postgrad Med. 2004 Oct-Dec;50(4):270-1.
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.
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。