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Translation of "motrice et sensorielle " (French → English) :
TERMINOLOGY
see also In-Context Translations below Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
Neuropathie héréditaire motrice et sensorielle
Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
Vessie neurogène:atonique (motrice) (sensorielle) | autonome | non-réflexe
Neuropathic bladder:atonic (motor)(sensory) | autonomous | nonreflex
WORLD HEALTH ORGANIZATION ICD-10: N31.2
WORLD HEALTH ORGANIZATION ICD-10: N31.2
Définition: Altération sévère du développement
de la coordination motrice, non imputable exclusivement à un retard mental global ou à une affection neurologique spécifique, congénitale ou acquise. Dans la plupart des cas, un examen clinique détaillé permet toutefois de mettre en évidence des signes traduisant une immaturité significative du développement neurologique, par exemple des mouvements choréiformes des membres, des syncinésies d'imitation, et d'autres signes moteurs associés, ainsi que des perturbations de la coordination motrice fine et globale. | Débilité motrice de l'enfant Dyspraxie de développement Trouble de l'acquisition
...[+++]de la coordination
Definition: A disorder in which the main feature is a serious impairment in the development of motor coordination that is not solely explicable in terms of general intellectual retardation or of any specific congenital or acquired neurological disorder. Nevertheless, in most cases a careful clinical examination shows marked neurodevelopmental immaturities such as choreiform movements of unsupported limbs or mirror movements and other associated motor features, as well as signs of impaired fine and gross motor coordination. | Clumsy child syndrome Developmental:coordination disorder | dyspraxia
WORLD HEALTH ORGANIZATION ICD-10: F82
WORLD HEALTH ORGANIZATION ICD-10: F82
agitation (motrice + mentale) | trouble du comportement alliant excitation mentale et motrice
agitation | anxiety
UGENT - Medical terms -
UGENT - Medical terms -
neuropathie ataxique sensorielle aigüe
Acute sensory ataxic Guillain-Barré syndrome
SNOMEDCT-BE (disorder) / 766049000
SNOMEDCT-BE (disorder) / 766049000
perte auditive sensorielle bilatérale
Bilateral sensory hearing loss
SNOMEDCT-BE (disorder) / 430985005
SNOMEDCT-BE (disorder) / 430985005
perte auditive sensorielle
Inner ear hearing loss
SNOMEDCT-BE (disorder) / 85571008
SNOMEDCT-BE (disorder) / 85571008
syndrome d'ataxie neuropathique sensorielle-dysarthrie-ophtalmoplégie
SANDO (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome
SNOMEDCT-BE (disorder) / 717266001
SNOMEDCT-BE (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome / 717266001
albinisme oculaire avec surdité sensorielle tardive
A rare X-linked inherited type of ocular albinism described in one African kindred (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately
SNOMEDCT-BE (disorder) / 722054007
SNOMEDCT-BE (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately / 722054007
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motrice et sensorielle
Date index:2022-02-19 -
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