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

Übersetzung für "Alcoholic cerebellar ataxia " (Englisch → Französisch) :

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

Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique


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

rédo-ataxie cérébelleuse


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

hérédo-ataxie cérébelleuse de Pierre Marie


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


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


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




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

Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X




Early-onset cerebellar ataxia

Ataxie cérébelleuse à début précoce




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'Alcoholic cerebellar ataxia' ->

Date index: 2022-05-02
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