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与特征表型相关的先天性免疫缺陷

Inborn errors of immunity associated with characteristic phenotypes.

机构信息

Centro Universitário Saúde ABC, Faculdade de Medicina, Serviço de Referência em Doenças Raras, Imunologia Clínica, Santo André, São Paulo, SP, Brazil.

Centro Universitário Saúde ABC, Faculdade de Medicina, Serviço de Referência em Doenças Raras, Imunologia Clínica, Santo André, São Paulo, SP, Brazil.

出版信息

J Pediatr (Rio J). 2021 Mar-Apr;97 Suppl 1(Suppl 1):S75-S83. doi: 10.1016/j.jped.2020.10.015. Epub 2020 Dec 19.

Abstract

OBJECTIVES

The aim of the report is to describe the main immunodeficiencies with syndromic characteristics according to the new classification of Inborn Errors of Immunity.

DATA SOURCE

The data search was centered on the PubMed platform on review studies, meta-analyses, systematic reviews, case reports and a randomized study published in the last 10 years that allowed the characterization of the several immunological defects included in this group.

DATA SYNTHESIS

Immunodeficiencies with syndromic characteristics include 65 immunological defects in 9 subgroups. The diversity of clinical manifestations is observed in each described disease and may appear early or later, with variable severity. Congenital thrombocytopenia, syndromes with DNA repair defect, immuno-osseous dysplasias, thymic defects, Hyper IgE Syndrome, anhidrotic ectodermal dysplasia with immunodeficiency and purine nucleoside phosphorylase deficiency were addressed.

CONCLUSIONS

Immunological defects can present with very different characteristics; however, the occurrence of infectious processes, autoimmune disorders and progression to malignancy may suggest diagnostic research. In the case of diseases with gene mutations, family history is of utmost importance.

摘要

目的

本报告旨在根据新的先天性免疫缺陷分类,描述具有综合征特征的主要免疫缺陷。

资料来源

数据检索集中在过去 10 年中发表的 PubMed 平台上的综述研究、荟萃分析、系统评价、病例报告和一项随机研究,这些研究允许对包括在该组中的几种免疫缺陷进行特征描述。

资料综合

具有综合征特征的免疫缺陷包括 9 个亚组中的 65 种免疫缺陷。在每个描述的疾病中都观察到临床表现的多样性,可能早期或晚期出现,严重程度不同。本文讨论了先天性血小板减少症、DNA 修复缺陷综合征、免疫骨发育不良、胸腺缺陷、高 IgE 综合征、无汗性外胚层发育不良伴免疫缺陷和嘌呤核苷磷酸化酶缺乏症。

结论

免疫缺陷可能表现出非常不同的特征;然而,感染过程、自身免疫性疾病和进展为恶性肿瘤的发生可能提示需要进行诊断研究。在有基因突变的疾病中,家族史至关重要。

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