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Brain disease
Early myoclonic encephalopathy
Encephalopathy
Encephalopathy due to COVID-19
Infantile epileptic dyskinetic encephalopathy
Myoclonic epilepsy in non-progressive encephalopathy
Toxic encephalopathy

Translation of "Toxic encephalopathy " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Toxic encephalopathy

encéphalopathie toxique
SNOMEDCT-BE (disorder) / 28394000
SNOMEDCT-BE (disorder) / 28394000


Toxic encephalopathy

Encéphalopathie toxique
WORLD HEALTH ORGANIZATION ICD-10: G92
WORLD HEALTH ORGANIZATION ICD-10: G92


Exophthalmic or toxic goitre NOS Graves' disease Toxic diffuse goitre

Goitre:exophtalmique ou toxique SAI | toxique diffus | Maladie de Basedow
WORLD HEALTH ORGANIZATION ICD-10: E05.0
WORLD HEALTH ORGANIZATION ICD-10: E05.0


encephalopathy | brain disease

encéphalopathie | affection du cerveau
UGENT - Medical terms -
UGENT - Medical terms -


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


Encephalopathy due to COVID-19

encéphalopathie par COVID-19
SNOMEDCT-BE (disorder) / 1240561000000108
SNOMEDCT-BE (disorder) / 1240561000000108


Infantile epileptic dyskinetic encephalopathy

encéphalopathie épileptique-dyskinétique infantile
SNOMEDCT-BE (disorder) / 771223000
SNOMEDCT-BE (disorder) / 771223000


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


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
IN-CONTEXT TRANSLATIONS


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'Toxic encephalopathy'

Date index:2022-01-04 -

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