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Brain localisation
CADASIL
CADASIL disease
CP
Cerebral localisation
Cerebral palsy
Hereditary multi-infarct type dementia
Little’s disease
Localised cerebral disease
Spastic paralysis

Traduction de «localised cerebral disease » (Anglais → Français) :



brain localisation | cerebral localisation

localisation cérébrale


Definition: Alzheimer's disease is a primary degenerative cerebral disease of unknown etiology with characteristic neuropathological and neurochemical features. The disorder is usually insidious in onset and develops slowly but steadily over a period of several years.

Définition: La maladie d'Alzheimer est une maladie cérébrale dégénérative primitive d'étiologie inconnue dont la neuropathologie et la neurochimie sont caractéristiques. Elle débute habituellement de façon insidieuse et progresse lentement mais régulièrement en quelques années.


Definition: Includes miscellaneous conditions causally related to brain disorder due to primary cerebral disease, to systemic disease affecting the brain secondarily, to exogenous toxic substances or hormones, to endocrine disorders, or to other somatic illnesses.

Définition: Comprend diverses affections causées par un trouble cérébral dû à une affection cérébrale primitive, à une affection somatique touchant secondairement le cerveau, à des substances toxiques exogènes ou des hormones, à des troubles endocriniens, ou à d'autres maladies somatiques.


Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,

ataxie spinocérébelleuse type 31


cerebral palsy | Little’s disease | spastic paralysis | CP [Abbr.]

infirmité motrice cérébrale | infirmité motrice d'origine cérébrale | insuffisance motrice d’origine cérébrale | paralysie cérébrale | IMC [Abbr.] | IMOC [Abbr.]


A rare disorder characterized by the combination of autoimmune intestinal disease, epileptic seizures and cerebral calcifications. Celiac disease and epilepsy manifest at a variable age. Celiac disease can present in a typical form with onset in the

syndrome de maladie coeliaque-calcifications cérébrales-épilepsie


CADASIL | CADASIL disease | cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | hereditary multi-infarct type dementia

CADASIL | syndrome CADASIL


Definition: Includes cases with a history of hypertension and foci of ischaemic destruction in the deep white matter of the cerebral hemispheres. The cerebral cortex is usually preserved and this contrasts with the clinical picture which may closely resemble that of dementia in Alzheimer's disease.

Définition: Démence vasculaire avec antécédent d'hypertension artérielle et de foyers de destruction ischémique dans la substance blanche profonde des hémisphères cérébraux. Le cortex cérébral est habituellement indemne, ce qui tranche avec le tableau clinique qui peut être proche de celui de la démence de la maladie d'Alzheimer.


A rare acquired eye disease with characteristics of progressive visual loss due to bilateral juxta foveolar capillary occlusions, capillary telangiectasia and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.

télangiectasie rétinienne juxtafovéolaire idiopathique occlusive




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Date index: 2021-12-08
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