Division of Paediatric Neurology, Department of Paediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.
Centre of Medical Genetics, Keio University, Tokyo, Japan.
J Clin Neurosci. 2020 Jan;71:289-292. doi: 10.1016/j.jocn.2019.08.111. Epub 2019 Sep 4.
Infantile neuroaxonal dystrophy 1 (INAD) (OMIM #256600) is a rare infantile onset neurodegenerative disease characterised by neuroregression and hypotonia, evolving into generalized spasticity, blindness and dementia. We report our diagnostic approach of a pair of siblings with psychomotor regression, hypotonia, optic atrophy and auditory neuropathy. The brain magnetic resonance imaging (MRI) showed progressive cerebellar atrophy. Genetic testing of the PLA2G6 confirmed presence of compound heterozygous novel mutations. As the variant c. 196C>T (p.Gln66X) was a truncating variant, it was considered as pathogenic while the variant c. 2249G>A (p. Cys750Tyr) was considered as "likely pathogenic" by bioinformatics analyses. Our patient expands the clinical phenotype of INAD as it described the first South-East Asian patient with INAD-associated auditory neuropathy. Our report highlights the importance of increased awareness of this condition amongst clinicians, the use of deep phenotyping using neuroimaging and the clinical utility of gene sequencing test in the delineation of syndromes associated with infantile neurodegenerative disease.
婴儿神经轴索性营养不良 1 型(INAD)(OMIM#256600)是一种罕见的婴儿期起病的神经退行性疾病,其特征为神经退行性变和肌张力低下,进而发展为全身性痉挛、失明和痴呆。我们报告了一对有精神运动倒退、肌张力低下、视神经萎缩和听神经病的同胞的诊断方法。脑部磁共振成像(MRI)显示进行性小脑萎缩。PLA2G6 的基因检测证实存在复合杂合新突变。由于变异 c.196C>T(p.Gln66X)是截断变异,因此被认为是致病性的,而变异 c.2249G>A(p.Cys750Tyr)通过生物信息学分析被认为是“可能致病性”的。我们的患者扩展了 INAD 的临床表型,因为它描述了第一个与 INAD 相关的听神经病的东南亚患者。我们的报告强调了临床医生对这种疾病的认识不断提高的重要性,使用神经影像学进行深度表型分析以及基因测序测试在描绘与婴儿神经退行性疾病相关的综合征方面的临床实用性。