Giulia Ferrera, Kevork Derderian, Rossella Izzo, Barbara Gnutti, Andrea Legati, Giovanna Zorzi, Eleonora Lamantea, Arcangela Iuso, Anna Ardissone
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引用次数: 0
摘要
致病性 WDR45 变体可导致神经发育障碍(NDDs),包括以发育迟缓(DD)、共济失调和锥体外系症状为特征的β-螺旋桨蛋白相关神经变性(BPAN)。我们的患者最初在 22 个月时出现发育迟缓,现在已经 7 岁了,表现为智力障碍、共济失调和僵直。核磁共振成像结果提示为利氏综合征,这是一种线粒体紊乱(MD)表型,但无脑铁积聚。在肌肉和成纤维细胞中发现呼吸链复合物 I (cI) 和复合物 II (cII) 活性降低,仅在肌肉中发现 cII 活性降低;但排除了原发性 MD 的可能。外显子组测序发现了一个新的致病WDR45变体。自噬通量分析表明,p62 反应轻度降低,自噬进展正常。这是第一份将 WDR45 与 cI 组装和活性联系起来的报告,表明线粒体功能障碍是一种潜在的病理生理 BPAN 机制。我们建议在诊断早发性NDD时考虑与WDR45相关的NDD,尤其是伴有cI缺乏的利格氏样脑病,即使没有脑铁积聚。
WDR45-related encephalopathy mimicking Leigh syndrome associated with complex I deficiency: a case report.
Pathogenic WDR45 variants cause neurodevelopmental disorders (NDDs) including β-propeller protein-associated neurodegeneration (BPAN), characterized by developmental delay (DD), ataxia and extrapyramidal signs. Our patient, initially presenting at 22 months with DD, now, aged 7, shows intellectual disability, ataxia and rigidity. MRI findings were suggestive of Leigh syndrome, a mitochondrial disorder (MD) phenotype, with no brain iron accumulation. Reduced activity of respiratory chain complex I (cI) and complex II (cII) was identified in muscle and fibroblasts, and a cII reduction in muscle only; however, a primary MD was excluded. Exome sequencing revealed a de novo pathogenic WDR45 variant. Autophagic flux analysis showed a mildly reduced p62 response, with normal autophagy progression. This is the first report linking WDR45 to cI assembly and activity, indicating mitochondrial dysfunction as a potential pathophysiological BPAN mechanism. We recommend considering WDR45-related NDDs when diagnosing early-onset NDDs, particularly Leigh-like encephalopathies with cI deficiency, even without brain iron accumulation.
期刊介绍:
The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community.
Key areas include:
-Monogenic and multifactorial disorders
-Development and malformation
-Hereditary cancer
-Medical Genomics
-Gene mapping and functional studies
-Genotype-phenotype correlations
-Genetic variation and genome diversity
-Statistical and computational genetics
-Bioinformatics
-Advances in diagnostics
-Therapy and prevention
-Animal models
-Genetic services
-Community genetics