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Additional lens
Attachment lens
Auxiliary lens
No-line bifocals
Omnifocal Lens
PAL
Progressive
Progressive addition lens
Progressive lens
Progressive multifocal lens
Progressive power lens
Progressive-addition bifocal
Supplementary lens
Varifocal lens

Translation of "Progressive addition lens " (English → French) :

progressive addition lens [ PAL | progressive lens | progressive | no-line bifocals ]

verre à foyer progressif [ verre progressif | progressif ]
Optical Glass
Verres d'optique


progressive multifocal lens | varifocal lens | progressive addition lens | Omnifocal Lens

verre à foyer progressif | verre progressif | verre varifocal | verre à variation de puissance | progressive
médecine > optométrie
médecine > optométrie


supplementary lens [ auxiliary lens | attachment lens | additional lens ]

lentille additionnelle [ lentille supplémentaire | lentille auxiliaire | bonnette | bonnette de mise au point ]
Photography | Optical Instruments
Photographie | Instruments d'optique


progressive power lens

lentille de contact à puissance progressive
Optical Glass | Visual Disorders
Verres d'optique | Troubles de la vision


progressive multifocal lens

lentille progressive multifocale
médecine > optométrie
médecine > optométrie


progressive-addition bifocal

verre à foyer progressif
IATE - Natural and applied sciences
IATE - Natural and applied sciences


additional lens

bonnette
photographie > objectif photographique
photographie > objectif photographique


Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001


A form of hereditary spastic paraplegia with onset usually in adulthood of progressive bilateral lower limb weakness and spasticity, sphincter dysfunction, decreased vibratory sense at the ankles and with additional manifestations including optical n

paraplégie spastique type 7
SNOMEDCT-BE (disorder) / 715776003
SNOMEDCT-BE (disorder) / 715776003


An extremely rare neurodegenerative disorder characterized by progressive spinocerebellar ataxia, sensorineural hearing loss, and hypergonadotropic hypogonadism associated with additional neurological manifestations (such as peripheral muscle wasting

syndrome de Richards-Rundle
SNOMEDCT-BE (such as peripheral muscle wasting / 715415005
SNOMEDCT-BE (disorder) / 715415005




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'Progressive addition lens'

Date index:2023-06-28 -

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