The clinical, radiological and genetic spectrum AARS2-related leukoencephalopathy: a case series of 15 patients and review of the literature

BACKGROUND: AARS2-related leukoencephalopathy is a rare autosomal recessive leukodystrophy with overlapping clinical and radiological features with CSF1R-related disease but distinct genetic and phenotypic characteristics. Since its description in 2014, fewer than 60 cases have been reported. METHODS: We conducted a multicentre retrospective case series of individuals with genetically confirmed AARS2-related leukoencephalopathy, integrating clinical, radiological, and molecular data from 15 newly identified patients. Neuroimaging was reviewed by experienced neuroradiologists, and variants were classified using ACMG criteria. A systematic literature review identified 56 additional cases. RESULTS: Across 71 individuals, mean age at onset was 27.3 years (range 0-57), with balanced sex distribution. Psychiatric and cognitive symptoms predominated early, affecting 70% and 86% of patients. Pyramidal signs (82%), gait disturbance (80%), and extrapyramidal motor features (45%) were common, whilst seizures occurred in 10%. Premature ovarian failure was reported in 82% of females. Sixteen individuals (22.5%) had childhood onset. Neuroimaging showed confluent frontoparietal white matter abnormalities, corpus callosum thinning, and multifocal diffusion abnormalities. Seventy-two unique AARS2 variants were identified, including seven novel variants. Missense variants predominated. Notably, variants previously linked only to infantile cardiomyopathy, including p.Arg592Trp, were observed. CONCLUSIONS: AARS2-related leukoencephalopathy is clinically and genetically heterogeneous with characteristic imaging and broad onset. Recognition of defining features is essential for diagnosis, and genomic testing should be prioritised. This study provides the most comprehensive characterisation to date and suggests genotype-phenotype separation between cardiomyopathy- and leukodystrophy-associated variants may not be absolute.

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Journal
Journal of Neurology
Published
2026-06-26
DOI
https://doi.org/10.1007/s00415-026-13964-1
Primary Topic
RNA regulation and disease
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article
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article

The clinical, radiological and genetic spectrum AARS2-related leukoencephalopathy: a case series of 15 patients and review of the literature

Anderson Rodrigues Brandão de Paiva, Paula Camila A.A.P. Matos, Jeremy Chataway, Katiane Sayão Souza Cabral et al.
Journal of Neurology
RNA regulation and disease
article

The clinical, radiological and genetic spectrum AARS2-related leukoencephalopathy: a case series of 15 patients and review of the literature

Anderson Rodrigues Brandão de Paiva, Paula Camila A.A.P. Matos, Jeremy Chataway, Katiane Sayão Souza Cabral, Paulo Ribeiro Nóbrega, Álvaro Ferreira, Pedro Maia Nobre Rocha Saffi, Fernando Kok, Charles Wade, Deborah Moreira Rangel, André Luiz Santos Pessoa, D. Lynch, J P Roberts, Lécio Figueira Pinto, Luiz Felipe Vasconcellos, Rumana Chowdhury, Matthew Adams, Tom Hayton, Ana C Martins Borges, Emília K. Embiruçu, Paula Brandão, Frederik Barkhof
article en

Abstract

BACKGROUND: AARS2-related leukoencephalopathy is a rare autosomal recessive leukodystrophy with overlapping clinical and radiological features with CSF1R-related disease but distinct genetic and phenotypic characteristics. Since its description in 2014, fewer than 60 cases have been reported. METHODS: We conducted a multicentre retrospective case series of individuals with genetically confirmed AARS2-related leukoencephalopathy, integrating clinical, radiological, and molecular data from 15 newly identified patients. Neuroimaging was reviewed by experienced neuroradiologists, and variants were classified using ACMG criteria. A systematic literature review identified 56 additional cases. RESULTS: Across 71 individuals, mean age at onset was 27.3 years (range 0-57), with balanced sex distribution. Psychiatric and cognitive symptoms predominated early, affecting 70% and 86% of patients. Pyramidal signs (82%), gait disturbance (80%), and extrapyramidal motor features (45%) were common, whilst seizures occurred in 10%. Premature ovarian failure was reported in 82% of females. Sixteen individuals (22.5%) had childhood onset. Neuroimaging showed confluent frontoparietal white matter abnormalities, corpus callosum thinning, and multifocal diffusion abnormalities. Seventy-two unique AARS2 variants were identified, including seven novel variants. Missense variants predominated. Notably, variants previously linked only to infantile cardiomyopathy, including p.Arg592Trp, were observed. CONCLUSIONS: AARS2-related leukoencephalopathy is clinically and genetically heterogeneous with characteristic imaging and broad onset. Recognition of defining features is essential for diagnosis, and genomic testing should be prioritised. This study provides the most comprehensive characterisation to date and suggests genotype-phenotype separation between cardiomyopathy- and leukodystrophy-associated variants may not be absolute.

Journal of NeurologyVol. 273(7)
Universidade Estadual do Ceará (BR), Universidade Federal do Rio de Janeiro (BR), University Hospitals Birmingham NHS Foundation Trust (GB), Universidade Federal do Ceará (BR), Leeds Teaching Hospitals NHS Trust (GB), National Institute for Health and Care Research (GB), Complexo Hospitalar Universitário Professor Edgard Santos (BR), Hospital Federal dos Servidores do Estado (BR), MRC Prion Unit (GB), Hospital Universitário de Brasília (BR), Mendelics (BR), Hospital Infantil Albert Sabin (BR), Faculdade de Medicina do ABC (BR), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR), Hospital Sírio-Libanês (BR), National Hospital for Neurology and Neurosurgery (GB), Amsterdam University Medical Centers (NL), Hospital Geral de Fortaleza (BR), Genomic (Brazil) (BR), University College London (GB)
Good health and well-being
Openalex Percentile: Top 11%
RNA regulation and disease
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