共济失调毛细血管扩张
肺炎
医学
共济失调
儿科
听力学
皮肤病科
遗传学
内科学
生物
精神科
DNA
DNA损伤
作者
Wafa Asmari,Saeed Al-Fadhil,Muhammad Shakir,Ahmed Albishri,Muhamed Fathi,Walid Muhammad
标识
DOI:10.29271/jcpsp.2020.10.1102
摘要
Ataxia-telangiectasia (A-T) is a genetically inherited disease, which is transmitted as an autosomal recessive disorder. There is a high incidence of consanguineous marriages in our area, so we believe that A-T may have higher incidence. A-T is characterised clinically by triad of cerebellar degeneration, telangiectasia, and immunodeficiency. We are reporting a 4-year girl with a novel genetic variant of AT, which is not reported before in local or international literature. She presented with necrotising pneumonia complicated by bronchopleural fistulae. She was treated successfully with antimicrobials and intravenous immunoglobulins and other supportive measures without surgical intervention. Key Words: Ataxia telangiectasia, Necrotising pneumonia, Bronchopleural fistulae.
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