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Bulbar palsy
Cortical dysarthria
Dumb rabies
Dysarthria
NMBA
Neuromuscular blocker
Neuromuscular blocking agent
Paralytic
Paralytic drug
Paralytic dysarthria
Paralytic flat foot
Paralytic flatfoot
Paralytic hydrophobia
Paralytic rabies
Paralytic squint
Paralytic strabismus
Pure anarthria
Speech defect
Sullen rabies

Translation of "Paralytic dysarthria " (English → French) :

paralytic dysarthria | bulbar palsy

dysarthrie paralytique | paralysie bulbaire
médecine > neurologie
médecine > neurologie


paralytic rabies | dumb rabies | sullen rabies | paralytic hydrophobia

rage paralytique | rage muette
médecine > infectiologie
médecine > infectiologie


paralytic strabismus [ paralytic squint ]

strabisme paralytique
Visual Disorders
Troubles de la vision


neuromuscular blocking agent [ NMBA | neuromuscular blocker | paralytic drug | paralytic ]

curarisant [ curare | bloqueur neuromusculaire ]
Nervous System | Muscles and Tendons | Medication
Système nerveux | Muscles et tendons | Médicaments


paralytic flatfoot [ paralytic flat foot ]

pied plat paralytique
Musculoskeletal System | Symptoms (Medicine)
Appareil locomoteur (Médecine) | Symptômes (Médecine)


SANDO (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome

syndrome d'ataxie neuropathique sensorielle-dysarthrie-ophtalmoplégie
SNOMEDCT-BE (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome / 717266001
SNOMEDCT-BE (disorder) / 717266001


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


Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001


cortical dysarthria | pure anarthria

dysarthrie corticale | anarthrie pure
médecine > neurologie
médecine > neurologie


dysarthria | speech defect

dysarthrie | difficulté d'élocution (due à des troubles moteurs)
UGENT - Medical terms -
UGENT - Medical terms -




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'Paralytic dysarthria'

Date index:2023-02-22 -

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