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Translation of "Cerebellar " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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
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
cerebellar | brain-related
cérébelleux | qui se rapporte au cervelet
UGENT - Medical terms -
UGENT - Medical terms -
A rare non-syndromic cerebellar malformation with characteristics of loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (normal cerebral hemispheres, fourth ventricle, pons, medulla and m
hypoplasie isolée unilatérale des hémisphères cérébelleux
SNOMEDCT-CA (normal cerebral hemispheres, fourth ventricle, pons, medulla and m / 766934006
SNOMEDCT-CA (trouble) / 766934006
Syndrome with characteristics of the onset of proximal tubulopathy in the first year of life, followed by progressive development during childhood of skin anomalies (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar atax
syndrome de tubulopathie proximale-diabète sucré-ataxie cérébelleuse
SNOMEDCT-BE (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar atax / 724062000
SNOMEDCT-BE (disorder) / 724062000
Disease with characteristics of early-onset of cerebellar signs with eye movement abnormalities and a very slow disease progression.Three families have been reported to date. Clinical manifestations include cerebellar signs (ataxia, dysarthria, and i
ataxie spinocérébelleuse type 5
SNOMEDCT-BE (ataxia, dysarthria, and i / 719302009
SNOMEDCT-BE (disorder) / 719302009
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
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
ataxie spinocérébelleuse type 15/16
SNOMEDCT-BE (disorder) / 716724006
SNOMEDCT-BE (disorder) / 716724006
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin
syndrome d'ataxie-photosensibilité-petite taille
SNOMEDCT-BE (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, sin / 773769008
SNOMEDCT-BE (disorder) / 773769008
Autosomal recessive cerebellar ataxia with late-onset spasticity
ataxie cérébelleuse autosomique récessive avec spasticité tardive
SNOMEDCT-BE (disorder) / 763348005
SNOMEDCT-BE (disorder) / 763348005
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'Cerebellar'
Date index:2021-11-18 -
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