Early-onset vasculitis: a toddler with ADA2 deficiency.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Mai M Abd Elhamed, Nermeen M Galal, Yasser Wali, Ilham Youssry
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引用次数: 0

Abstract

Deficiency of adenosine deaminase 2 (DADA2) is an autoinflammatory disease caused by autosomal recessive inherited loss of function mutations in the adenosine deaminase 2 (ADA2) encoding gene, which reduces plasma ADA2 concentration levels.ADA2 has a major role in the maturation and differentiation of the immune system. It ensures immune homeostasis with the help of adenosine receptors on the cell surface because ADA2 acts as an extracellular enzyme that has an important role in regulating extracellular adenosine concentration and mediates cellular immune interactions. We report a fatal outcome of an infant with DADA2 as a result of delayed diagnosis and definitive treatment with bone marrow transplantation.

早发性血管炎:ADA2缺乏的幼儿。
腺苷脱氨酶2 (DADA2)缺乏症是由常染色体隐性遗传的腺苷脱氨酶2 (ADA2)编码基因的功能突变缺失引起的一种自身炎症性疾病,其降低了血浆ADA2浓度水平。ADA2在免疫系统的成熟和分化中起着重要作用。ADA2作为一种胞外酶,在调节胞外腺苷浓度和介导细胞免疫相互作用方面起着重要作用,因此在细胞表面腺苷受体的帮助下确保免疫稳态。我们报告了一名患有DADA2的婴儿由于延迟诊断和骨髓移植的最终治疗而死亡的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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