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A New DARS2 Mutation Discovered in an Adult Patient

par Ikazabo, Rosy R.N.G.N.G.;Mostosi, Christian;Jissendi, Patrice;Labaisse, Marie Anne;Vandernoot, Isabelle
Référence Case Reports in Neurology, page (107-113)
Publication Publié, 2020

Article révisé par les pairs

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Résumé :

We report a case of an adult patient suffering from leukoencephalopathy with brainstem and spinal cord involvement and elevated white matter lactate (LBSL) caused by a DARS2 polymorphism. DARS2 mutation was identified by combining MRI and genetic analysis. Our patient was affected by compound heterozygosity for a pathogenic mutation and a common variant, but with reduced aspartyl-tRNA synthetase activity. Brain and spinal cord magnetic resonance imaging revealed extensive white matter abnormalities; spectroscopy revealed no lactate elevation. A new compound heterozygous DARS2 variant combined with a polymorphism in the other allele in an adult patient with LBSL was identified, resulting in reduced DARS2 activity. This combination is rare and has consequences on how we should consider benign variant polymorphisms in the future.