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Bulbar motor neuron disease
Bulbar neuron
Bulbar paralysis
Distal
Duchenne's paralysis
Duchenne's syndrome
Fazio-Londe
Kennedy disease
Kennedy's disease
Kugelberg-Welander
Labioglossolaryngeal paralysis
Nerve cell
Neuron
Neuronal ceroid lipofuscinosis
Neurone
Primary
Progressive bulbar palsy
Progressive bulbar palsy of childhood
Progressive bulbar paralysis
SBMA
Scapuloperoneal form
Spinal and bulbar muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy adult form
Spinobulbar muscular atrophy
X-linked spinal and bulbar muscular atrophy

Translation of "Bulbar neuron " (English → French) :

bulbar neuron

neurone bulbaire
IATE - Health
IATE - Health


Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy

Amyotrophie spinale progressive Dégénérescence familiale du neurone moteur Paralysie bulbaire progressive Sclérose latérale:amyotrophique | primitive
WORLD HEALTH ORGANIZATION ICD-10: G12.2
WORLD HEALTH ORGANIZATION ICD-10: G12.2


Bulbar motor neuron disease

sclérose latérale amyotrophique
SNOMEDCT-BE (disorder) / 86044005
SNOMEDCT-BE (disorder) / 86044005


bulbar paralysis | Duchenne's paralysis | Duchenne's syndrome | labioglossolaryngeal paralysis | progressive bulbar palsy | progressive bulbar paralysis

paralysie bulbaire | paralysie bulbaire progressive
IATE - Health
IATE - Health


spinal and bulbar muscular atrophy | SBMA | Kennedy disease | X-linked spinal and bulbar muscular atrophy | spinobulbar muscular atrophy | Kennedy's disease

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique


A very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic intranuclear inclusions in neuronal and glial cells, and neuronal loss. Infantile, juvenile, and adult-onset cases have been described. As any part of th

maladie des inclusions intranucléaires neuronales
SNOMEDCT-BE (disorder) / 715437003
SNOMEDCT-BE (disorder) / 715437003


A variant of central neurocytoma, a rare neuronal neoplasm, composed of round cells with neuronal differentiation, which is located outside of the ventricular system, usually within the spinal cord or cerebral hemispheres and that manifests with head

neurocytome extraventriculaire
SNOMEDCT-BE (disorder) / 716787002
SNOMEDCT-BE (disorder) / 716787002


nerve cell | neuron | neurone

neurone
IATE - Health
IATE - Health


Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

Amyotrophie spinale (de):adulte | distale | enfant, type II | forme juvénile, type III [Kugelberg-Welander] | forme scapulo-péronière | Paralysie bulbaire progressive de l'enfant [Fazio-Londe]
WORLD HEALTH ORGANIZATION ICD-10: G12.1
WORLD HEALTH ORGANIZATION ICD-10: G12.1


Neuronal ceroid lipofuscinosis

Lipofuscinose à céroïdes neuronaux
WORLD HEALTH ORGANIZATION ICD-10: E75.4
WORLD HEALTH ORGANIZATION ICD-10: E75.4




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'Bulbar neuron'

Date index:2022-12-24 -

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