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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