病例报告:在一个2岁男孩身上早期出现遗传性血管的症状
Jurate Staikuniene-Kozonis1,2, Juste Staikunaite2,3, Edita Gasiuniene1
1Department of Immunology and Allergology, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Frontiers in pediatrics
|July 9, 2024
概括
遗传性血管炎 (HAE) 由于C1抑制剂缺乏,可以在生命的很早阶段显现. 遗传咨询对于及时诊断和治疗受影响家庭的HAE至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 免疫学 免疫学 免疫学
- 儿科 儿科 儿科
背景情况:
- 遗传性血管 (HAE) 是一种罕见的自体主导性疾病,与C1抑制剂 (C1-INH) 缺乏或功能障碍有关.
- 在SERPING1基因的突变导致C1-INH缺陷 (HAE类型I和II),而F12基因突变与HAE类型III有关.
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