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AIDP
Acute autoimmune neuropathy
Acute idiopathic facial neuropathy
Acute idiopathic polyneuritis
Acute idiopathic polyradiculoneuritis
Acute inflammatory demyelinating polyneuropathy
Acute inflammatory polyneuropathy
Acute inflammatory polyradiculoneuropathy
Bell palsy
Bell's palsy
CMT
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
GBS
Guillain-Barré syndrome
Guillain-Barré-Strohl syndrome
HMSN
Hereditary and idiopathic neuropathy
Hereditary motor and sensory neuropathy
Herpetic facial paralysis
Idiopathic facial paralysis
Idiopathic peripheral autonomic neuropathy
Infectious polyneuritis
LGBS
LHON
Landry's paralysis
Landry-Guillain-Barré Syndrome
Leber's disease
Leber's hereditary optic atrophy
Leber's hereditary optic neuropathy
Leber's optic atrophy
Leber's optic neuropathy
Other hereditary and idiopathic neuropathies
PMA
Peroneal muscular atrophy

Vertaling van "hereditary and idiopathic neuropathy " (Engels → Frans) :

Hereditary and idiopathic neuropathy

Neuropathie héréditaire et idiopathique


Other hereditary and idiopathic neuropathies

Autres neuropathies héréditaires et idiopathiques


Bell palsy [ Bell's palsy | idiopathic facial paralysis | herpetic facial paralysis | acute idiopathic facial neuropathy ]

paralysie de Bell [ maladie de Bell | paralysie faciale a frigore | paralysie faciale idiopathique | paralysie faciale essentielle | paralysie faciale périphérique ]


acute autoimmune neuropathy | acute idiopathic polyneuritis | acute idiopathic polyradiculoneuritis | acute inflammatory demyelinating polyneuropathy | acute inflammatory demyelinating polyradiculoneuropathy | acute inflammatory polyneuropathy | acute inflammatory polyradiculoneuropathy | Guillain-Barré syndrome | Guillain-Barré-Strohl syndrome | infectious polyneuritis | Landry-Guillain-Barré Syndrome | Landry's paralysis | AIDP [ ...[+++]

polyradiculonévrite aiguë | polyradiculonévrite aiguë inflammatoire | polyradiculonévrite curable | syndrome de Guillain-Barré


Leber's hereditary optic atrophy [ Leber's optic atrophy | Leber's disease | Leber's optic neuropathy ]

maladie de Leber [ atrophie optique de Leber | atrophie optique héréditaire et familiale ]


Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]

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


Leber's hereditary optic neuropathy | LHON [Abbr.]

maladie de Leber | neuropathie optique de Leber


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

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


A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyeliti

neuropathie sensitivo-motrice axonale héréditaire avec acrodystrophie


Idiopathic peripheral autonomic neuropathy

neuropathie autonome périphérique idiopathique


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