期刊文献+

常染色体显性遗传STAT1基因功能获得性变异免疫缺陷病二例

Two Chinese cases with STAT1 gene gain-of-function variation
原文传递
导出
摘要 2例患儿分别为7岁3月龄男童、1岁3月龄女童,分别以“反复咳嗽、咳痰、吞咽困难”和“发热、左侧腋下淋巴结肿大、口腔溃疡”起病。例1主要表现为反复肺炎、中耳炎、支气管扩张、慢性皮肤黏膜念珠菌病和身材矮小,例2主要表现为全身播散性结核病和口腔念珠菌病。2例患儿均有血液系统表现,例1既往有噬血细胞综合征病史,入院后血细胞分析示贫血,例2全血细胞减少,直接抗人球蛋白实验和抗血小板抗体阳性;2例患儿c-ANCA均阳性,例2胰岛素自身抗体及胰岛细胞抗体阳性。2例患儿基因检测均为STAT1基因杂合变异,核苷酸变化为c.1154 C>T,氨基酸改变p.T385M,诊断为STAT1基因功能获得性变异免疫缺陷。
作者 陈兰勤 刘军 姚瑶 殷菊 贺建新 徐保平 Chen Lanqin;Liu Jun;Yao Yao;Yin Ju;He Jianxin;Xu Baoping(China National Clinical Research Center for Respiratory Diseases,Department of Resiratory Diseases,Beijing Children′s Hospital,Capital Medical University,National Center for Children′s Health,Beijing 100045,China)
出处 《中华儿科杂志》 CAS CSCD 北大核心 2021年第8期700-702,共3页 Chinese Journal of Pediatrics
  • 相关文献

参考文献3

二级参考文献25

  • 1陈同辛,王玺.原发性免疫缺陷病诊断标准[J].实用儿科临床杂志,2006,21(9):573-576. 被引量:38
  • 2YamazakiY, YamadaM, KawaiT, et al.Two novel gain–of–function mutations of STAT1 responsible for chronic mucocutaneous candidiasis di–sease:impaired production of IL–17A and IL–22, and the presence of anti–IL–17F autoantibody[J].J Immunol, 2014, 193(10):4880-4887.DOI: 10.4049/jimmunol.1401467.
  • 3NielsenJ, Kofod-OlsenE, SpaunE, et al.A STAT1–gain–of–function mutation causing Th17 deficiency with chronic mucocutaneous candidiasis, psoriasiform hyperkeratosis and dermatophytosis[J].BMJ Case Rep, 2015, pii:bcr2015211372.DOI: 10.1136/bcr-2015-211372.
  • 4RichardsCS, BaleS, BellissimoDB, et al.ACMG recommendations for standards for interpretation and reporting of sequence variations:revisions 2007[J].Genet Med, 2008, 10(4):294-300.DOI: 10.1097/GIM.0b013e31816b5cae.
  • 5TanimuraM, DohiK, HirayamaM, et al.Recurrent inflammatory aortic aneurysms in chronic mucocutaneous candidiasis with a gain–of–function STAT1 mutation[J].Int J Cardiol, 2015, 196:88-90.DOI: 10.1016/j.ijcard.2015.05.183.
  • 6WildbaumG, ShaharE, KatzR, et al.Continuous G–CSF therapy for isolated chronic mucocutaneous candidiasis:complete clinical remission with restoration of IL–17 secretion[J].J Allergy Clin Immunol, 2013, 132(3):761-764.DOI: 10.1016/j.jaci.2013.04.018.
  • 7van de VeerdonkFL, KoenenHJ, van Der VeldenWJ, et al.Immunotherapy with G–CSF in patients with chronic mucocutaneous candidiasis[J].Immunol Lett, 2015, 167(1):54-56.DOI: 10.1016/j.imlet.2015.05.008.
  • 8LanternierF, CypowyjS, PicardC, et al.Primary immunodeficiencies underlying fungal infections[J].Curr Opin Pediatr, 2013, 25(6):736-747.DOI: 10.1097/MOP.0000000000000031.
  • 9HoriT, OhnishiH, TeramotoT, et al.Autosomal–dominant chronic mucocutaneous candidiasis with STAT1–mutation can be complicated with chronic active hepatitis and hypothyroidism[J].J Clin Immunol, 2012, 32(6):1213-1220.DOI: 10.1007/s10875-012-9744-6.
  • 10UzelG, SampaioEP, LawrenceMG, et al.Dominant gain–of–function STAT1 mutations in FOXP3 wild–type immune dysregulation–polyendocrinopathy–enteropathy–X–linked–like syndrome[J].J Allergy Clin Immunol, 2013, 131(6):1611-1623.DOI: 10.1016/j.jaci.2012.11.054.

共引文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部