| Literature DB >> 33260297 |
Adriana Vargas1, Jorge Rojas2, Ivan Aivasovsky3, Sergio Vergara3, Marianna Castellanos3, Carolina Prieto3, Luis Celis3.
Abstract
The KARS gene encodes the aminoacyl-tRNA synthetase (aaRS), which activates and joins the lysin with its corresponding transfer RNA (tRNA) through the ATP-dependent aminoacylation of the amino acid. KARS gene mutations have been linked to diverse neurologic phenotypes, such as neurosensorial hearing loss, leukodystrophy, microcephaly, developmental delay or regression, peripheral neuropathy, cardiomyopathy, the impairment of the mitochondrial respiratory chain, and hyperlactatemia, among others. This article presents the case of a Colombian pediatric patient with two pathological missense variants in a compound heterozygous state in the KARS gene and, in addition to the case report, the paper reviews the literature for other cases of KARS1-associated leukodystrophy.Entities:
Keywords: KARS gene; aminoacylation; epilepsy; hearing loss developmental delay; leukodystrophy; whole exome sequencing
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Year: 2020 PMID: 33260297 PMCID: PMC7759888 DOI: 10.3390/genes11121437
Source DB: PubMed Journal: Genes (Basel) ISSN: 2073-4425 Impact factor: 4.096