Optic atrophy (Q41885): Difference between revisions
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Atrofias ópticas se referem a um grupo específico de neuropatias ópticas hereditárias em que a causa da disfunção do nervo óptico é herdada, seja em um padrão autossômico dominante ou autossômico recessivo. Atrofia óptica autossômica dominante (AOAD), tipo Kjer, é a atrofia óptica mais comum, enquanto a atrofia óptica autossômica recessiva (AOAR) é uma forma rara. | |||
| description / en | description / en | ||
Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal recessive optic atrophy (AROA) is a rare form. | |||
Revision as of 08:12, 13 August 2026
Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal recessive optic atrophy (AROA) is a rare form.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 9C40.B |
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| English | Optic atrophy |
Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal recessive optic atrophy (AROA) is a rare form. |
