A Novel Combination of Biallelic Variants in the VARS2 Gene: A Severe Phenotype
To our knowledge, only 29 individuals have been described in the literature with biallelic pathogenic variants in the valyl-tRNA synthetase 2 (VARS2) gene, responsible for changes in the mitochondrial respiratory chain complex. We report two siblings with a novel combination of biallelic variants in the VARS2 gene (c.1079C>T p.Ala360Val, likely pathogenic, and c.1258G>A p.Ala420Thr, likely pathogenic). Both presented early hypertrophic cardiomyopathy and lactic acidosis, with fatal outcomes within the first year of life. The first also presented severe fetal growth restriction and a ventricular septal defect; the second developed epilepsy, respiratory failure, and psychomotor delay. This genotype may be linked to a particularly severe cardiac phenotype. Our report broadens the clinical and genetic spectrum of VARS2-related mitochondrial disease, highlights the variability of phenotypic expression, and reinforces the importance of early molecular diagnosis in neonatal-onset cardiomyopathy. Genetic confirmation enables accurate genetic counselling and consideration of prenatal or preimplantation diagnosis in future pregnancies.
Authors
- Inês Almeida (ORCID: https://orcid.org/0000-0002-5029-1972)
- M R Maria Clarissa Rodrigues
- Mariana Reis
- Joana Capela (ORCID: https://orcid.org/0000-0002-5081-5481)
- Patrícia Lipari (ORCID: https://orcid.org/0000-0001-9197-7586)
- Ana Ramalho
- Marta Novo (ORCID: https://orcid.org/0000-0001-5522-0914)
Institutions
- University of Lisbon (PT)
- Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
- Algarve Biomedical Center (PT)
- Hospital de Santa Maria (PT)
- University of Algarve (PT)
Publication Details
- Journal
- Acta Médica Portuguesa
- Published
- 2026-05-18
- DOI
- https://doi.org/10.20344/amp.23831
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00