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.

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Journal
Acta Médica Portuguesa
Published
2026-05-18
DOI
https://doi.org/10.20344/amp.23831
Primary Topic
Mitochondrial Function and Pathology
Type
article
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article

A Novel Combination of Biallelic Variants in the VARS2 Gene: A Severe Phenotype

Inês Almeida, M R Maria Clarissa Rodrigues, Mariana Reis, Joana Capela et al.
Acta Médica Portuguesa
Mitochondrial Function and Pathology
article

A Novel Combination of Biallelic Variants in the VARS2 Gene: A Severe Phenotype

Inês Almeida, M R Maria Clarissa Rodrigues, Mariana Reis, Joana Capela, Patrícia Lipari, Ana Ramalho, Marta Novo
article en

Abstract

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.

Acta Médica Portuguesa
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)
Good health and well-being
Openalex Percentile: Top 9%
Mitochondrial Function and Pathology
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