An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia-live.demo.openlinksw.com

This disease is characterised by progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter

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  • This disease is characterised by progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter (en)
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  • LBSL is inherited in an autosomal recessive fashion (en)
dbp:causes
  • Mutation in a gene DARS2 (en)
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  • 1 (xsd:integer)
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  • Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation (en)
dbp:onset
  • Adolescence (en)
dbp:specialty
  • Neurology (en)
dbp:symptoms
  • Progressive cerebellar ataxia (en)
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rdfs:label
  • Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (en)
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