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Alcoholic cerebellar ataxia
Cerebellar ataxia
Cerebral degeneration
Degeneration
Dysfunction of autonomic nervous system due to alcohol
Early-onset cerebellar ataxia with essential tremor
Encephalopathy
Hunt's ataxia
Myoclonus
Retained tendon reflexes

Translation of "Alcoholic cerebellar ataxia " (English → French) :

Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
https://icd.who.int/browse10/2 (...) (...) [HTML]
Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique
WORLD HEALTH ORGANIZATION ICD-10: G31.2
WORLD HEALTH ORGANIZATION ICD-10: G31.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
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
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ataxie type Caïman
SNOMEDCT-BE (disorder) / 717332007
SNOMEDCT-BE (disorder) / 717332007
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https://browser.ihtsdotools.or (...) [HTML]
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
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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
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https://browser.ihtsdotools.or (...) [HTML]
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
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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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https://browser.ihtsdotools.or (...) [HTML]
A rare subtype of type 1 autosomal dominant cerebellar ataxia with characteristics of cerebellar ataxia, tremor and cognitive impairment. Prevalence is unknown. Fewer than 80 patients affected by the disease have been identified to date. Age of onset
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ataxie spinocérébelleuse type 15/16
SNOMEDCT-BE (disorder) / 716724006
SNOMEDCT-BE (disorder) / 716724006
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https://browser.ihtsdotools.or (...) [HTML]
Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia
https://icd.who.int/browse10/2 (...) (...) [HTML]
Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X
WORLD HEALTH ORGANIZATION ICD-10: G11.1
WORLD HEALTH ORGANIZATION ICD-10: G11.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon
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syndrome d'ataxie cérébelleuse autosomique récessive-saccade oculaire
SNOMEDCT-BE (increased tendon / 766814006
SNOMEDCT-BE (disorder) / 766814006
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https://browser.ihtsdotools.or (...) [HTML]
A very rare progressive and untreatable disease with manifestations of ataxia with sensory neuropathy. Prevalence is unknown, typically starts in middle-aged adults and presents with cerebellar ataxia, pyramidal signs, and peripheral sensory loss. Th
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ataxie spinocérébelleuse type 4
SNOMEDCT-BE (disorder) / 715755008
SNOMEDCT-BE (disorder) / 715755008
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https://browser.ihtsdotools.or (...) [HTML]
Autosomal recessive cerebellar ataxia with late-onset spasticity
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ataxie cérébelleuse autosomique récessive avec spasticité tardive
SNOMEDCT-BE (disorder) / 763348005
SNOMEDCT-BE (disorder) / 763348005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Cerebellar ataxia
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ataxie cérébelleuse
SNOMEDCT-BE (disorder) / 85102008
SNOMEDCT-BE (disorder) / 85102008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : cerebellar ataxia    hunt's ataxia    cerebral degeneration    degeneration    encephalopathy    myoclonus    retained tendon reflexes    Alcoholic cerebellar ataxia    


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'Alcoholic cerebellar ataxia'

Date index:2021-09-08 -

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