原发性免疫缺陷伴严重多器官免疫失调。

Pub Date : 2019-12-28 eCollection Date: 2019-01-01 DOI:10.1155/2019/8746249
Tatyana Gavrilova
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引用次数: 1

摘要

1型多腺体自身免疫综合征,也称为自身免疫性多内分泌病-念珠菌病-外胚层营养不良(APECED),是一种罕见的多器官累及的原发性免疫缺陷疾病。除了易患严重危及生命的感染外,APECED患者还容易继发于严重自身免疫的器官损害。由于这是一种常染色体隐性遗传病,AIRE基因的双等位基因突变是APECED的原因。作者提出一例APECED与一个单一的AIRE突变。全外显子组测序确定了BTNL2基因的突变,作者认为这可能导致了患者的表现。
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Primary Immunodeficiency with Severe Multi-Organ Immune Dysregulation.

Polyglandular autoimmune syndrome type 1, also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), is a rare primary immunodeficiency disorder with multi-organ involvement. Besides for being predisposed to severe life-threatening infections, patients with APECED are also prone to organ impairment secondary to severe autoimmunity. As this is an autosomal recessive disorder, a biallelic mutation in the AIRE gene is responsible for APECED. The author presents a case of APECED with a single AIRE mutation. Whole exome sequencing identified a mutation in the BTNL2 gene that the author suggests may have contributed to the patient's presentation.

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