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Translation of "encephalopathy " (English → French) :
TERMINOLOGY
see also In-Context Translations below encephalopathy | brain disease
encéphalopathie | affection du cerveau
UGENT - Medical terms -
UGENT - Medical terms -
Toxic encephalopathy
encéphalopathie toxique
SNOMEDCT-BE (disorder) / 28394000
SNOMEDCT-BE (disorder) / 28394000
Encephalopathy due to COVID-19
encéphalopathie par COVID-19
SNOMEDCT-BE (disorder) / 1240561000000108
SNOMEDCT-BE (disorder) / 1240561000000108
A Wernicke-like encephalopathy with characteristics of seizures responsive to high doses of thiamine. Two cases have been described so far. Clinical features include epilepsy, nystagmus, ophthalmoplegia and ataxia. The disease results from mutations
encéphalopathie sensible à la thiamine
SNOMEDCT-BE (disorder) / 723557004
SNOMEDCT-BE (disorder) / 723557004
A rare genetic disorder of thiamine metabolism and transport with characteristics of the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneu
polyneuropathie progressive avec nécrose striatale bilatérale
SNOMEDCT-BE (disorder) / 771305006
SNOMEDCT-BE (disorder) / 771305006
Myoclonic epilepsy in non-progressive encephalopathy
epilepsie myoclonique des encéphalopathies non-progressives
SNOMEDCT-BE (disorder) / 778047006
SNOMEDCT-BE (disorder) / 778047006
Early myoclonic encephalopathy
encéphalopathie myoclonique précoce
SNOMEDCT-BE (disorder) / 44423001
SNOMEDCT-BE (disorder) / 44423001
A rare inborn error of metabolism characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dys
encéphalopathie associée à une hyperméthioninémie par déficit en adénosine kinase
SNOMEDCT-BE (disorder) / 763721006
SNOMEDCT-BE (disorder) / 763721006
Infantile epileptic dyskinetic encephalopathy
encéphalopathie épileptique-dyskinétique infantile
SNOMEDCT-BE (disorder) / 771223000
SNOMEDCT-BE (disorder) / 771223000
Inherited disorder characterized by episodes of metabolic crisis and acute encephalopathy. Life-threatening episodes manifest with poor feeding, vomiting, weight loss, lethargy, tachypnea, seizures or coma and are caused by hyperammonemia, metabolic
encéphalopathie hyperammoniémique par déficit en anhydrase carbonique VA
SNOMEDCT-BE (disorder) / 764456001
SNOMEDCT-BE (disorder) / 764456001
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'encephalopathy'
Date index:2022-06-15 -
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