Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Genetics, University Medical Centre Groningen, Groningen, The Netherlands.
Eur J Hum Genet. 2020 Jun;28(6):763-769. doi: 10.1038/s41431-020-0600-5. Epub 2020 Mar 10.
Previously, intragenic CAMTA1 copy number variants (CNVs) have been shown to cause non-progressive, congenital ataxia with or without intellectual disability (OMIM#614756). However, ataxia, intellectual disability, and dysmorphic features were all incompletely penetrant, even within families. Here, we describe four patients with de novo nonsense, frameshift or missense CAMTA1 variants. All four patients predominantly manifested features of ataxia and/or spasticity. Borderline intellectual disability and dysmorphic features were both present in one patient only, and other neurological and behavioural symptoms were variably present. Neurodevelopmental delay was found to be mild. Our findings indicate that also nonsense, frameshift and missense variants in CAMTA1 can cause a spastic ataxia syndrome as the main phenotype.
先前,研究已经表明基因内 CAMTA1 拷贝数变异(CNVs)可导致非进行性、先天性共济失调伴或不伴智力障碍(OMIM#614756)。然而,即使在家族内,共济失调、智力障碍和发育异常的表现也不完全外显。在这里,我们描述了 4 例具有新生无义、移码或错义 CAMTA1 变异的患者。这 4 例患者主要表现为共济失调和/或痉挛的特征。仅 1 例患者存在轻度智力障碍和发育异常特征,其他神经和行为症状也存在不同程度的表现。发现神经发育迟缓是轻度的。我们的研究结果表明,CAMTA1 中的无义、移码和错义变异也可引起以痉挛性共济失调为主要表型的综合征。