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Identifying high-risk neurological phenotypes in adult-onset classic monogenic autoinflammatory diseases: when should neurologists consider testing?
BMC Neurology ( IF 2.6 ) Pub Date : 2024-04-17 , DOI: 10.1186/s12883-024-03621-3
Guilherme Diogo Silva , João Vitor Mahler , Sérgio Roberto Pereira da Silva Junior , Leonardo Oliveira Mendonça , Pedro Lucas Grangeiro de Sá Barreto Lima , Paulo Ribeiro Nóbrega , Fernando Kok , Fernando Freua

Monogenic autoinflammatory disorders result in a diverse range of neurological symptoms in adults, often leading to diagnostic delays. Despite the significance of early detection for effective treatment, the neurological manifestations of these disorders remain inadequately recognized. We conducted a systematic review searching Pubmed, Embase and Scopus for case reports and case series related to neurological manifestations in adult-onset monogenic autoinflammatory diseases. Selection criteria focused on the four most relevant adult-onset autoinflammatory diseases—deficiency of deaminase 2 (DADA2), tumor necrosis factor receptor associated periodic fever syndrome (TRAPS), cryopyrin associated periodic fever syndrome (CAPS), and familial mediterranean fever (FMF). We extracted clinical, laboratory and radiological features to propose the most common neurological phenotypes. From 276 records, 28 articles were included. The median patient age was 38, with neurological symptoms appearing after a median disease duration of 5 years. Headaches, cranial nerve dysfunction, seizures, and focal neurological deficits were prevalent. Predominant phenotypes included stroke for DADA2 patients, demyelinating lesions and meningitis for FMF, and meningitis for CAPS. TRAPS had insufficient data for adequate phenotype characterization. Neurologists should be proactive in diagnosing monogenic autoinflammatory diseases in young adults showcasing clinical and laboratory indications of inflammation, especially when symptoms align with recurrent or chronic meningitis, small vessel disease strokes, and demyelinating lesions.

中文翻译:

识别成人发病的经典单基因自身炎症性疾病的高风险神经表型:神经科医生何时应考虑进行检测?

单基因自身炎症性疾病会导致成人出现多种神经系统症状,常常导致诊断延迟。尽管早期检测对于有效治疗具有重要意义,但这些疾病的神经系统表现仍未得到充分认识。我们进行了一项系统综述,在 Pubmed、Embase 和 Scopus 中检索与成人发病的单基因自身炎症性疾病的神经系统表现相关的病例报告和病例系列。选择标准侧重于四种最相关的成人发病的自身炎症性疾病——脱氨酶 2 缺乏症 (DADA2)、肿瘤坏死因子受体相关周期性发热综合征 (TRAPS)、冷热蛋白相关周期性发热综合征 (CAPS) 和家族性地中海热 (FMF) 。我们提取了临床、实验室和放射学特征,提出了最常见的神经表型。 276 条记录中,收录了 28 篇文章。患者中位年龄为 38 岁,中位病程 5 年后出现神经系统症状。头痛、脑神经功能障碍、癫痫发作和局灶性神经功能缺损很常见。主要表型包括 DADA2 患者的中风、FMF 患者的脱髓鞘病变和脑膜炎以及 CAPS 患者的脑膜炎。 TRAPS 没有足够的数据来充分表征表型。神经科医生应积极诊断年轻人的单基因自身炎症性疾病,显示出炎症的临床和实验室指征,特别是当症状与复发性或慢性脑膜炎、小血管病中风和脱髓鞘病变一致时。
更新日期:2024-04-17
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