你为什么打自己? 全外体序列测序诊断为单源性自身免疫的诊断
Lina M Castano-Jaramillo1, Francisco Rivas Larrauri, Selma C Scheffler-Mendoza
1Clinical Immunology Department, Instituto Nacional de Pediatria, Mexico City, Mexico.dr.lugo.reyes@gmail.com.
Journal of genetics
|December 11, 2023
概括
基因检测在超过一半的患有严重自身免疫性疾病的儿科患者中发现了单一的原因. 这凸显了在复杂的自身免疫病例中,特别是儿童中,考虑免疫的先天性错误的重要性.
科学领域:
- 免疫学 免疫学 免疫学
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
背景情况:
- 免疫的先天性错误 (IEI) 通常表现为自身免疫和自身炎症.
- 确定这些疾病的遗传基础对于诊断和管理至关重要.
研究的目的:
- 识别儿科患者自身免疫性疾病的潜在单一性原因.
- 调查整个外体序列测序在诊断具有自身免疫性的IEI中的实用性.
主要方法:
- 在26名患有自身免疫性疾病的儿科患者身上进行了全外组测序.
- 患者选择标准包括家族病史,早期发病,治疗耐药性或相关感染.
主要成果:
- 在54%的病例中,与患者的表型相容的遗传变异被确定.
- 这表明单一的原因在严重的儿科自身免疫性疾病中起着重要作用.
结论:
- 在患有严重,耐治疗或复杂自身免疫性疾病的年轻患者中,应怀疑免疫的先天性错误,特别是当与感染相关时.
- 整体外因子测序是诊断儿童自身免疫性疾病的单基因原因的有效工具.
相关概念视频
Autoimmune Disorders
447
Autoimmune diseases are a group of disorders in which the body's immune system mistakenly attacks its own cells, tissues, and organs. This results from an overactive immune response against substances and tissues normally present in the body. Let's delve into the concept and mechanism of autoimmune diseases from an immune system point of view, explore different causes and examples of such diseases, and discuss potential solutions.
Concept and Mechanism of Autoimmune Diseases
The immune...
Concept and Mechanism of Autoimmune Diseases
The immune...
447
Genome-wide Association Studies-GWAS
13.5K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
13.5K
Pleiotropy
40.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.5K


