ATP1A3相关疾病的扩展表型:一个病例系列。

Child neurology open Pub Date : 2021-11-03 eCollection Date: 2021-01-01 DOI:10.1177/2329048X211048068
Jelena De Vrieze, Ingrid M B H van de Laar, Johanneke F de Rijk-van Andel, Erik-Jan Kamsteeg, Irene A W Kotsopoulos, Stella A de Man
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引用次数: 1

摘要

由ATP1A3基因突变引起的神经系统疾病最初被报道为三种不同的罕见临床综合征:儿童期交替偏瘫(AHC)、快速发作性肌张力障碍帕金森病(RDP)和小脑性共济失调、反射性松弛、弓形足、视肌萎缩和感音神经性听力损失(CAPOS)。在这个病例系列中,我们描述了3名患者。一位母亲和她的女儿表现出一种不同的中间表型,具有相同的杂合错义突变(p.[R756C]),最近被文献描述为复发性脑病伴小脑共济失调(RECA)。此外,第三名患者表现出中间AHC-RDP表型,并可能具有致病性新发错义突变(p.[L100 V])。这些患者支持了越来越多的证据,即AHC, RDP和RECA是持续的ATP1A3突变谱的一部分,该突变谱仍在扩大。三个共同特征是突然发作,神经系统症状不对称,以及触发因素的存在。目前,作者主张在早期阶段进行外显子组测序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expanding Phenotype of <i>ATP1A3</i> - Related Disorders: A Case Series.

Expanding Phenotype of ATP1A3 - Related Disorders: A Case Series.

Neurologic disorders caused by mutations in the ATP1A3 gene were originally reported as three distinct rare clinical syndromes: Alternating Hemiplegia of Childhood (AHC), Rapid-onset Dystonia Parkinsonism (RDP) and Cerebellar ataxia, Areflexia, Pes cavus, Opticus atrophy and Sensorineural hearing loss (CAPOS). In this case series, we describe 3 patients. A mother and her daughter showed an intermediate phenotype different from each other with the same heterozygous missense mutation (p.[R756C]), recently described in literature as Relapsing Encephalopathy With Cerebellar Ataxia (RECA). In addition, a third patient showed an intermediate AHC-RDP phenotype and had a likely pathogenic novel de novo missense mutation (p.[L100 V]). These patients support the growing evidence that AHC, RDP and RECA are part of a continuous ATP1A3 mutation spectrum that is still expanding. Three common features were a sudden onset, asymmetrical neurological symptoms, as well as the presence of triggering factors. When present, the authors argue to perform exome sequencing in an early stage.

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