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Translation of "cerebellar degeneration " (English → French) :
TERMINOLOGY
see also In-Context Translations below Cerebellar degeneration
dégénérescence cérébelleuse
SNOMEDCT-BE (disorder) / 95646004
SNOMEDCT-BE (disorder) / 95646004
Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
ataxie spinocérébelleuse type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008
Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique
WORLD HEALTH ORGANIZATION ICD-10: G31.2
WORLD HEALTH ORGANIZATION ICD-10: G31.2
Hereditary cerebellar:ataxia NOS | degeneration | disease | syndrome
Ataxie SAI | Dégénérescence | Maladie | Syndrome | cérébelleux (cérébelleuse) héréditaire
WORLD HEALTH ORGANIZATION ICD-10: G11.9
WORLD HEALTH ORGANIZATION ICD-10: G11.9
Cerebellar ataxia Cayman type has characteristics of psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia. The prevalence
ataxie type Caïman
SNOMEDCT-BE (disorder) / 717332007
SNOMEDCT-BE (disorder) / 717332007
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies / 765747004
SNOMEDCT-BE (disorder) / 765747004
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante B
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m / 765745007
SNOMEDCT-BE (disorder) / 765745007
Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy
Dégénérescence (de):Junius-Kuhnt | maculaire sénile (atrophique) (exsudative) | Druses (dégénératives) | Kyste | Plis | Stries angioïdes | Trou | de la macula | Maculopathie toxique
WORLD HEALTH ORGANIZATION ICD-10: H35.3
WORLD HEALTH ORGANIZATION ICD-10: H35.3
A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006
A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on
ataxie spinocérébelleuse type 26
SNOMEDCT-BE (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on / 718769009
SNOMEDCT-BE (disorder) / 718769009
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'cerebellar degeneration'
Date index:2021-12-11 -
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