| Literature DB >> 30635318 |
Anudeep Yelam1, Elanagan Nagarajan2, Miguel Chuquilin3, Raghav Govindarajan1.
Abstract
Leucoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) is a very rare autosomal recessive, slowly progressive neurological disorder characterised by distinctive clinical findings including cerebellar, pyramidal and dorsal column dysfunction. This is caused by a mutation in the DARS2 gene, which encodes mitochondrial aspartyl-tRNA synthetase. MRI shows distinctive abnormalities in the cerebral white matter and specific brain stem and spinal cord tracts. Here, we present a case of LBSL, with a novel c.1192-2A>G mutation. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: muscle disease; neuro genetics; neuroimaging; neuromuscular disease
Mesh:
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Year: 2019 PMID: 30635318 PMCID: PMC6340551 DOI: 10.1136/bcr-2018-227755
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X