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Idiopathique
Maladie de Bell
Paralysie de Bell
Paralysie facial périphérique
Paralysie faciale
Paralysie faciale
Paralysie faciale a frigore
Paralysie faciale complète
Paralysie faciale congénitale héréditaire isolée
Paralysie faciale essentielle
Paralysie faciale idiopathique
Paralysie faciale périphérique
Paralysie faciale périphérique de Bell
Paralysie faciale périphérique idiopathique familiale
Paralysie faciale à frigore

Translation of "Paralysie faciale périphérique " (French → English) :

paralysie faciale périphérique de Bell | paralysie faciale périphérique | paralysie de Bell | paralysie faciale à frigore | paralysie faciale complète

Bell's palsy | facial palsy | Bell's paralysis | facial paralysis
médecine
médecine


paralysie faciale périphérique idiopathique familiale

recurrent facioplegia
IATE - Health
IATE - Health


paralysie faciale périphérique

peripheral facial paralysis
IATE - Health
IATE - Health


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

Bell palsy [ Bell's palsy | idiopathic facial paralysis | herpetic facial paralysis | acute idiopathic facial neuropathy ]
Système nerveux | Maladies humaines diverses
Nervous System | Human Diseases - Various


paralysie facialriphérique

peripheral facioplegia
IATE - Health
IATE - Health


paralysie faciale

facial paralysis
Système nerveux
Nervous System


syndrome de paralysie faciale congénitale héréditaire-surdité variable

An extremely rare autosomal recessive disorder with characteristics of bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears) and strabismus.
SNOMEDCT-BE (disorder) / 722389002
SNOMEDCT-BE (midfacial retrusion, low-set ears) and strabismus. / 722389002


Paralysie faciale (de):Bell | idiopathique

Facial palsy
WORLD HEALTH ORGANIZATION ICD-10: G51.0
WORLD HEALTH ORGANIZATION ICD-10: G51.0


paralysie faciale congénitale héréditaire isolée

An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002


paralysie faciale

Facial palsy
SNOMEDCT-BE (disorder) / 280816001
SNOMEDCT-BE (disorder) / 280816001




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Paralysie faciale périphérique

Date index:2024-02-26 -

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