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Atrophy of the optic nerve
Autosomal dominant optic atrophy Kjer type
Autosomal dominant optic atrophy type 3
Encephalitis+
Infantile spinal muscular atrophy
Leber's disease
Leber's hereditary optic atrophy
Leber's optic atrophy
Leber's optic neuropathy
Meningitis+
Optic atrophy
Optic atrophy+
Polyneuropathy+
Primary optic atrophy
Progressive muscular atrophy of infancy
Retrobulbar neuritis+
SMA I
Severe infantile spinal muscular atrophy
Simple optic atrophy
Spinal muscular atrophy type I
Syphilitic parkinsonism+
Werdnig-Hoffman disease

Traduction de «optic atrophy » (Anglais → Français) :

primary optic atrophy [ simple optic atrophy ]

atrophie optique primitive [ atrophie optique primaire | atrophie par atteinte primitive du nerf optique ]


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 ]


atrophy of the optic nerve | optic atrophy

atrophie du nerf optique


A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

syndrome de Wolfram-like






Autosomal dominant optic atrophy type 3

syndrome d'atrophie optique-cataracte autosomique dominante


Charcot's arthropathy+ (M14.6*) Late syphilitic:acoustic neuritis+ (H94.0*) | encephalitis+ (G05.0*) | meningitis+ (G01*) | optic atrophy+ (H48.0*) | polyneuropathy+ (G63.0*) | retrobulbar neuritis+ (H48.1*) | Syphilitic parkinsonism+ (G22*) Tabes dorsalis

Arthropathie de Charcot+ (M14.6*) Atrophie optique+ (H48.0*) | Encéphalite+ (G05.0*) | Méningite+ (G01*) | Névrite:acoustique+ (H94.0*) | rétrobulbaire+ (H48.1*) | Polynévrite+ (G63.0*) | syphilitique tardive | Parkinsonisme syphilitique+ (G22*) Tabès


Autosomal dominant optic atrophy Kjer type

atrophie optique autosomique dominante classique


infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann


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