Literature DB >> 17665025

Leukoencephalopathy with brainstem and spinal cord involvement and high brain lactate: report of three Brazilian patients.

Daniel Gurgel Fernandes Távora1, Mauro Nakayama, Rômulo Lopes Gama, Thereza Cristina de Lara Alvim, Dalton Portugal, Enio Alberto Comerlato.   

Abstract

A novel leukoencephalopathy was recently identified based on magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy ((1)H-MRS) findings. Leukoencephalopathy with brainstem and spinal cord involvement and high lactate (LBSL) is an autosomal recessive disorder characterized by early onset of symptoms and slowly progressive cerebellar, pyramidal and spinal cord dorsal column dysfunction. MRI and (1)H-MRS typically show abnormalities within cerebral and cerebellar white matter, a characteristic involvement of brainstem and spinal cord tracts and elevated lactate in the abnormal white matter. We present three cases with characteristic clinical and neuroimaging findings of this disorder. Some additional unique findings of our patients are discussed, like distal motor neuropathy and elevated creatine kinase in the serum.

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Year:  2007        PMID: 17665025     DOI: 10.1590/s0004-282x2007000300028

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  4 in total

1.  Leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation: a novel mutation in the DARS2 gene.

Authors:  Anudeep Yelam; Elanagan Nagarajan; Miguel Chuquilin; Raghav Govindarajan
Journal:  BMJ Case Rep       Date:  2019-01-10

2.  Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene.

Authors:  Charalampos Tzoulis; Gia Tuong Tran; Ivar Otto Gjerde; Jan Aasly; Gesche Neckelmann; Jana Rydland; Viktoria Varga; Pia Wadel-Andersen; Laurence A Bindoff
Journal:  J Neurol       Date:  2011-07-27       Impact factor: 4.849

3.  Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL.

Authors:  Nurun Nahar Borna; Yoshihito Kishita; Norio Sakai; Yusuke Hamada; Koji Kamagata; Masakazu Kohda; Akira Ohtake; Kei Murayama; Yasushi Okazaki
Journal:  Genes (Basel)       Date:  2020-11-09       Impact factor: 4.096

Review 4.  Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination.

Authors:  Amena Smith Fine; Christina L Nemeth; Miriam L Kaufman; Ali Fatemi
Journal:  J Neurodev Disord       Date:  2019-12-16       Impact factor: 4.025

  4 in total

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