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PedAM

Pediatric Disease Annotations & Medicines




Disease encephalopathy
Phenotype C0023264|subacute necrotising encephalopathy
Sentences 2
PubMedID- 26016801 As with classical leigh syndrome, affected lsfc patients suffered from a severe neurological disorder characterised by subacute necrotising encephalopathy, but also presented with microvesicular steatosis (morin et al 1993), likely due to the low levels of cox activity in the liver of patients (merante et al 1993).
PubMedID- 20843336 Leigh syndrome [1], also termed as subacute necrotising encephalopathy is a rare, inherited progressive neurodegenerative disorder with characteristic pathological features usually presenting in infancy or early childhood.

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