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CPEO
Chronic progressive external ophthalmoplegia
PSP
Progressive external ophthalmoplegia
Progressive supranuclear ophthalmoplegia
Progressive supranuclear palsy
Steele-Richardson-Olszewski
Steele-Richardson-Olszewski syndrome
Supranuclear ophthalmoplegia

Translation of "progressive supranuclear ophthalmoplegia " (English → French) :

Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]

Ophtalmoplégie supranucléaire progressive [maladie de Steele-Richardson-Olszewski]
WORLD HEALTH ORGANIZATION ICD-10: G23.1
WORLD HEALTH ORGANIZATION ICD-10: G23.1


supranuclear ophthalmoplegia

ophtalmoplégie supranucléaire | paralysie des mouvements associés des yeux
médecine > neurologie
médecine > neurologie


progressive supranuclear palsy [ PSP | Steele-Richardson-Olszewski syndrome ]

paralysie supranucléaire progressive [ PSP | maladie de Steele-Richardson-Olszewski | syndrome de Steele-Richardson-Olszewski ]
Nervous System | Human Diseases - Various
Système nerveux | Maladies humaines diverses


chronic progressive external ophthalmoplegia | CPEO [Abbr.]

ophtalmoplégie externe progressive chronique
IATE - Health
IATE - Health


Progressive external ophthalmoplegia

Ophtalmoplégie externe progressive
WORLD HEALTH ORGANIZATION ICD-10: H49.4
WORLD HEALTH ORGANIZATION ICD-10: H49.4


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'OEP-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009


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


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009




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'progressive supranuclear ophthalmoplegia'

Date index:2024-03-16 -

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