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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease leigh syndrome
Comorbidity C0023264|subacute necrotizing encephalomyelopathy
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PubMedID- 21749722 leigh syndrome (ls, omim 256000) is a subacute necrotizing encephalomyelopathy characterized by bilateral symmetrical necrotic lesions of gray matter nuclei in the basal ganglia, diencephalon, cerebellum or brainstem.
PubMedID- 20593000 The rare subacute necrotizing encephalomyelopathy was first described by leigh [1] as a clinically and etiologically highly variable, progressive syndrome seen particularly in pediatric population although a few juvenile and adult cases are known [2, 3].

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