患有干扰素马受体1缺乏症的患者的系统性阿斯伯吉洛斯;一个病例报告
Hossein Esmaeilzadeh1,2, Zahra Chavoshzadeh3, Seyed Hesamedin Nabavizadeh1,2
1Division of Allergy and Clinical Immunology, Department of Pediatrics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
BMC pediatrics
|June 5, 2023
概括
与IFNGR1突变相关的干扰素马受体 (IFNGR) 缺陷可能导致严重的阿斯伯吉洛症. 这一案例凸显了在患有侵入性真菌感染的患者中考虑IFNGR缺乏的重要性.
科学领域:
- 免疫学 免疫学 免疫学
- 遗传学 是一个遗传学.
- 传染性疾病 传染性疾病
背景情况:
- 干扰素马受体 (IFNGR) 缺陷包括IFNGR1,IFNGR2和STAT1的突变,导致免疫缺陷 (27A/B).
- 患者容易受到菌根,病毒 (Herpesviridae) 和细菌 (李斯特菌,沙门氏菌) 感染.
- SH2B3突变与自身免疫和淋巴增殖性疾病有关.
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