| Literature DB >> 27502409 |
Fabian Baertling1, Bader Alhaddad2, Annette Seibt1, Sonja Budaeus1, Thomas Meitinger2,3,4, Tim M Strom2,3, Ertan Mayatepek1, Jörg Schaper5, Holger Prokisch2,3, Tobias B Haack2,3, Felix Distelmaier6.
Abstract
VARS2 encodes a mitochondrial aminoacyl-tRNA-synthetase. Mutations in VARS2 have recently been identified as a cause of mitochondrial encephalomyopathy in three individuals. However, clinical information remained scarce. Exome sequencing lead us to identify compound heterozygous pathogenic VARS2 variants in a boy presenting with severe lactic acidosis, hypertrophic cardiomyopathy, epilepsy, and abnormalities on brain imaging including hypoplasia of corpus callosum and cerebellum as well as a massive lactate peak on MR-spectroscopy. Studies in patient-derived fibroblasts confirmed the functional relevance of the identified VARS2 variants. Our report expands the phenotypic spectrum associated with this rare mitochondrial defect, in that VARS2 deficiency may also cause severe neonatal presentations with cardiac involvement and structural brain abnormalities.Entities:
Keywords: Aminoacyl tRNA synthtetase; Cardiomyopathy; Mitochondrial disease; OXPHOS; VARS2
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Year: 2016 PMID: 27502409 DOI: 10.1007/s11011-016-9890-2
Source DB: PubMed Journal: Metab Brain Dis ISSN: 0885-7490 Impact factor: 3.584