Department of Pediatrics, Emory University School of Medicine, 2015 Uppergate Drive, Atlanta, GA, 30322, USA.
Neurosciences Research, Children's Healthcare of Atlanta, Georgia, USA.
Sci Rep. 2020 Sep 30;10(1):16184. doi: 10.1038/s41598-020-73219-5.
Pure sensory polyneuropathy of genetic origin is rare in childhood and hence important to document the clinical and genetic etiologies from single or multi-center studies. This study focuses on a retrospective chart-review of neurological examinations and genetic and electrodiagnostic data of confirmed sensory polyneuropathy in subjects at a tertiary-care Children's Hospital from 2013 to 2019. Twenty subjects were identified and included. Neurological examination and electrodiagnostic testing showed gait-difficulties, absent tendon reflexes, decreased joint-position, positive Romberg's test and large fiber sensory polyneuropathy on sensory nerve conduction studies in all patients associated with lower-extremity spasticity (6), cardiac abnormalities or cardiomyopathy (5), developmental delay (4), scoliosis (3), epilepsy (3) and hearing-difficulties (2). Confirmation of genetic diagnosis in correlation with clinical presentation was obtained in all cases (COX20 n = 2, HADHA n = 2, POLG n = 1, FXN n = 4, ATXN2 n = 3, ATM n = 3, GAN n = 2, SPG7 n = 1, ZFYVE26 n = 1, FH n = 1). Our single-center study shows genetic sensory polyneuropathies associated with progressive neurodegenerative disorders such as mitochondrial ataxia, Friedreich ataxia, spinocerebellar ataxia type 2, ataxia telangiectasia, spastic paraplegia, giant axonal neuropathy, and fumarate hydratase deficiency. We also present our cohort data in light of clinical features reported for each gene-specific disease subtype in the literature and highlight the importance of genetic testing in the relevant clinical context of electrophysiological findings of peripheral sensory polyneuropathy.
遗传性纯感觉性多发性神经病在儿童中较为罕见,因此有必要通过单中心或多中心研究来记录其临床和遗传病因。本研究专注于回顾性分析 2013 年至 2019 年在一家三级儿童医院确诊的感觉性多发性神经病患者的神经学检查、遗传学和电诊断数据。共确定并纳入了 20 名患者。所有患者的神经学检查和电诊断检查均显示步态困难、腱反射消失、关节位置降低、Romberg 试验阳性和感觉神经传导研究显示大纤维感觉性多发性神经病,同时伴有下肢痉挛(6 例)、心脏异常或心肌病(5 例)、发育迟缓(4 例)、脊柱侧凸(3 例)、癫痫(3 例)和听力障碍(2 例)。所有病例均通过与临床表现相关的基因诊断得到证实(COX20 n = 2、HADHA n = 2、POLG n = 1、FXN n = 4、ATXN2 n = 3、ATM n = 3、GAN n = 2、SPG7 n = 1、ZFYVE26 n = 1、FH n = 1)。我们的单中心研究显示,遗传性感觉性多发性神经病与进行性神经退行性疾病有关,如线粒体共济失调、弗里德里希共济失调、脊髓小脑性共济失调 2 型、共济失调毛细血管扩张症、痉挛性截瘫、巨大轴索性神经病和富马酸水合酶缺乏症。我们还根据文献中每种基因特异性疾病亚型的临床特征报告了我们的队列数据,并强调了在相关临床背景下进行电生理学检查结果提示的外周感觉性多发性神经病的基因检测的重要性。