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Traduction de «hereditary motor » (Anglais → Français) :

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 demyelination and axonal degeneration in nerve biopsies. It presents with m

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maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante B

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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

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maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C

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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

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maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D

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Hereditary motor and sensory neuropathy

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Neuropathie héréditaire motrice et sensorielle

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amyotrophie péronière de Charcot-Marie-Tooth | CMT | maladie de Charcot-Marie-Tooth | neuropathie héréditaire de Charcot-Marie-Tooth

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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

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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

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hereditary nephropathy | Alport's syndrome | hereditary haematuria associated with nerve deafness and ocular changes | hereditary hematuria associated with nerve deafness and ocular changes | hereditary nephropathy with haematuria | familial hereditary nephropathy | haematuric familial nephropathy

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néphropathie familiale avec surdité | syndrome d'Alport | néphrite hématurique héréditaire avec surdité | néphrite chronique héréditaire

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hereditary disposition | hereditary predisposition

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disposition héréditaire | prédisposition héréditaire

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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

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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 mot ...[+++]

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D'autres ont cherché : alport's syndrome bessel-hagen disease charcot-marie-tooth disease déjerine-sottas hereditary motor and sensory neuropathy dyspraxia familial hereditary nephropathy haematuric familial nephropathy hereditary deforming chondrodysplasia hereditary disposition hereditary multiple exostosis hereditary nephropathy hereditary nephropathy with haematuria hereditary predisposition multiple cartilaginous exostoses multiple exostosis multiple osteochondromas peroneal muscular atrophy hereditary motor

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Date index: 2023-05-10