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1
Yao syndrome in a child with C2 deficiency.一名患有C2缺陷的儿童出现姚氏综合征。
J Allergy Clin Immunol Pract. 2024 Nov;12(11):3159-3162. doi: 10.1016/j.jaip.2024.08.018. Epub 2024 Aug 14.
2
Genetic polymorphisms of HLA class III and GLO1 in Chinese Yao nationality.中国瑶族人群中HLAⅢ类基因和GLO1基因的遗传多态性
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J Tongji Med Univ. 1990;10(1):37-42. doi: 10.1007/BF02909120.
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World J Gastroenterol. 2019 Sep 14;25(34):5134-5151. doi: 10.3748/wjg.v25.i34.5134.
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Short stature in primary school students belonging to a minority ethnic group of Yao in China.中国瑶族少数民族小学生身材矮小。
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[Comparative study of three common G6PD gene mutations in Yao and Han People in Guangxi].广西瑶族和汉族三种常见G6PD基因突变的比较研究
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本文引用的文献

1
Genetically transitional disease: conceptual understanding and applicability to rheumatic disease.遗传过渡性疾病：概念理解及其在风湿性疾病中的适用性。
Nat Rev Rheumatol. 2024 May;20(5):301-310. doi: 10.1038/s41584-024-01086-9. Epub 2024 Feb 28.
2
Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome.经典补体途径中联合遗传缺陷与系统性红斑狼疮和原发性干燥综合征风险的强烈关联。
Arthritis Rheumatol. 2022 Nov;74(11):1842-1850. doi: 10.1002/art.42270. Epub 2022 Oct 7.
3
Expansion of Phenotypic and Genotypic Spectrum in Yao Syndrome: A Case Series.姚综合征表型和基因型谱的扩展：病例系列。
J Clin Rheumatol. 2022 Jan 1;28(1):e156-e160. doi: 10.1097/RHU.0000000000001655.
4
Primary immune regulatory disorders: a growing universe of immune dysregulation.原发性免疫调节紊乱：一个不断增长的免疫调节紊乱领域。
Curr Opin Allergy Clin Immunol. 2020 Dec;20(6):582-590. doi: 10.1097/ACI.0000000000000689.
5
Novel Pathogenic C2 Variant Associated with Disseminated GBS Infection.与播散性GBS感染相关的新型致病性C2变体
J Clin Immunol. 2020 May;40(4):662-664. doi: 10.1007/s10875-020-00784-9. Epub 2020 May 8.
6
Alterations in nucleotide-binding oligomerization domain-2 expression, pathway activation, and cytokine production in Yao syndrome.姚综合征中核苷酸结合寡聚化结构域-2 表达、途径激活和细胞因子产生的改变。
Autoimmunity. 2018 Mar;51(2):53-61. doi: 10.1080/08916934.2018.1442442. Epub 2018 Feb 22.
7
A Systematic Analysis of Treatment and Outcomes of NOD2-Associated Autoinflammatory Disease.NOD2相关自身炎症性疾病的治疗与结局的系统分析
Am J Med. 2017 Mar;130(3):365.e13-365.e18. doi: 10.1016/j.amjmed.2016.09.028. Epub 2016 Oct 28.
8
A new category of autoinflammatory disease associated with NOD2 gene mutations.一种与 NOD2 基因突变相关的新型自身炎症性疾病。
Arthritis Res Ther. 2011;13(5):R148. doi: 10.1186/ar3462. Epub 2011 Sep 14.

Yao syndrome in a child with C2 deficiency.

作者信息

Cresoe-Ortiz Samantha, Hall Geoffrey, Randell Rachel L, Lawrence Monica G, Patel Aarat, Peroutka Christina, Yao Qingping, Mousallem Talal

机构信息

Department of Pediatrics, Division of Pediatric Allergy and Immunology, Duke University School of Medicine, Durham, NC.

Department of Pediatrics, Division of Pediatric Rheumatology, Duke University School of Medicine, Durham, NC.

出版信息

J Allergy Clin Immunol Pract. 2024 Nov;12(11):3159-3162. doi: 10.1016/j.jaip.2024.08.018. Epub 2024 Aug 14.

DOI:10.1016/j.jaip.2024.08.018
PMID:39151691
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11750179/
Abstract
摘要