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Cervical neuritis
Dyspraxia
Encephalitis+
Meningitis+
Motor neuritis
Nerve inflammation
Neuritis
Optic atrophy+
Polyneuropathy+
Retrobulbar neuritis+
Syphilitic parkinsonism+

Translation of "motor neuritis " (English → French) :

Motor neuritis

neuropathie motrice périphérique
SNOMEDCT-BE (disorder) / 95663000
SNOMEDCT-BE (disorder) / 95663000


Charcot's arthropathy+ (M14.6*) Late syphilitic:acoustic neuritis+ (H94.0*) | encephalitis+ (G05.0*) | meningitis+ (G01*) | optic atrophy+ (H48.0*) | polyneuropathy+ (G63.0*) | retrobulbar neuritis+ (H48.1*) | Syphilitic parkinsonism+ (G22*) Tabes dorsalis

Arthropathie de Charcot+ (M14.6*) Atrophie optique+ (H48.0*) | Encéphalite+ (G05.0*) | Méningite+ (G01*) | Névrite:acoustique+ (H94.0*) | rétrobulbaire+ (H48.1*) | Polynévrite+ (G63.0*) | syphilitique tardive | Parkinsonisme syphilitique+ (G22*) Tabès
WORLD HEALTH ORGANIZATION ICD-10: A52.1
WORLD HEALTH ORGANIZATION ICD-10: A52.1


Cervical neuritis

névrite brachiale (cervicale)
SNOMEDCT-BE (cervical) neuritis (disorder) / 267977009
SNOMEDCT-BE (cervicale) / 267977009


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 ch ...[+++]

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 ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F82
WORLD HEALTH ORGANIZATION ICD-10: F82


neuritis | nerve inflammation

névrite | névrite (= inflammation d'un nerf)
UGENT - Medical terms -
UGENT - Medical terms -


A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuro

ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale
SNOMEDCT-BE (e.g. impaired gait, dysarthria) and mild motor peripheral neuro / 725464001
SNOMEDCT-BE (disorder) / 725464001


A rare neuroinflammatory disease characterized by the onset of ataxia, dysarthria and cerebral white matter changes that are triggered by viral infection. Episodic progressive neurodegeneration (manifesting with loss of motor and verbal skills, muscl

maladie neurodégénérative fatale post-virale
SNOMEDCT-BE (manifesting with loss of motor and verbal skills, muscl / 774206008
SNOMEDCT-BE (disorder) / 774206008


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C
SNOMEDCT-BE (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too / 765746008
SNOMEDCT-BE (disorder) / 765746008


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies / 765747004
SNOMEDCT-BE (disorder) / 765747004


An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c

maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type B
SNOMEDCT-BE (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c / 773330000
SNOMEDCT-BE (disorder) / 773330000




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'motor neuritis'

Date index:2022-01-20 -

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