Subacute necrotizing encephalomyelopathy, or Leigh syndrome (LS), is a progressive neurodegenerative disorder characterized by psychomotor retardation, feeding difficulties, intermittent abnormalities of the respiratory rhythm, cranial palsies, and ataxia, with onset usually in infancy or early childhood (1). filexlib. Introduction. Leigh syndrome (LS, also known as subacute necrotising encephalopathy) is an early-onset neurodegenerative disease, characterised by basal ganglia, brain stem, and thalamus change but with considerable clinical and genetic heterogeneity.1, 2 The estimated incidence of LS is 1:40 000 live births.3 Most frequently, LS manifests in the central nervous system as psychomotor Introduction. Leigh syndrome is a neurodegenerative disorder caused by mitochondrial dysfunction with both phenotypic and genetic heterogeneity. 1 Leigh syndrome is characterized by: (i) neurodegenerative disease with variable symptoms due to (ii) mitochondrial impairment caused by a hereditary genetic defect accompanied by (iii) bilateral central nervous system lesions that can be associated
The Online Mendelian Inheritance in Man Database (OMIM 2014) defines Leigh syndrome as: (1) a neurodegenerative disease with variable symptoms, (2) caused by mitochondrial dysfunction from a hereditary genetic defect, and (3) accompanied by bilateral central nervous system (CNS) lesions.
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