Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol

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WORLD HEALTH ORGANIZATION ICD-10: G31.2

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congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome

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hérédo-ataxie cérébelleuse

IATE - Health

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Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia

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hérédo-ataxie cérébelleuse de Pierre Marie

IATE - Health

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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

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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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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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cerebellar ataxia

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ataxie cérébelleuse

Nervous System

Système nerveux

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Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

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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

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acute cerebellar ataxia

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ataxie cérébelleuse aiguë

IATE - Health

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Early-onset cerebellar ataxia

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Ataxie cérébelleuse à début précoce

WORLD HEALTH ORGANIZATION ICD-10: G11.1

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Others have searched : early-onset cerebellar ataxia hunt's ataxia marie ataxia marie disease marie's ataxia marie's cerebellar ataxia marie's disease nonne-marie sydrome acute cerebellar ataxia cerebellar ataxia cerebral degeneration congenital cerebellar ataxia degeneration encephalopathy myoclonus retained tendon reflexes Alcoholic cerebellar ataxia

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'Alcoholic cerebellar ataxia'

Date index:2022-07-01 -

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