Literature DB >> 30325133

The first pediatric case of leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) from Turkey.

Dilek Çavuşoğlu1, Nihal Olgaç-Dündar1, Özgür Öztekin2, Taha Reşid Özdemir3, Pınar Arıcan4, Pınar Gençpınar1.   

Abstract

Çavuşoğlu D, Olgaç-Dündar N, Öztekin Ö, Özdemir TR, Arıcan P, Gençpınar P. The first pediatric case of leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) from Turkey. Turk J Pediatr 2018; 60: 216-220. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) is defined as an autosomal recessive inheritance disorder characterized by slowly progressive cerebellar, pyramidal and dorsal column dysfunction. The diagnosis is based on specific magnetic resonance imaging abnormalities (MRI) in the cerebral and cerebellar white matter and selective involvement of white matter tracts in the brain stem and spinal cord. LBSL is caused by mutations in the DARS2 gene which encodes the mitochondrial aspartyl-tRNA synthetase. Herein, we report the first pediatric case from Turkey with a typical MRI course of LBSL associated with a compound heterozygous mutation in DARS2 gene.

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Keywords:  DARS2; LBSL; MRI; leukoencephalopathy; mitochondrial

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Year:  2018        PMID: 30325133     DOI: 10.24953/turkjped.2018.02.018

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia.

Authors:  Martje G Pauly; Yorck Hellenbroich; Kathrin Grundmann-Hauser; Frauke Hinrichs; Katja Lohmann; Norbert Brüggemann
Journal:  Mov Disord Clin Pract       Date:  2021-06-14
  1 in total

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