Autosomal dominant optic atrophy plus syndrome (Q94807): Difference between revisions
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Atrofia óptica autossômica dominante síndrome plus é uma forma de atrofia óptica autossômica dominante que associa atrofia óptica a outras manifestações clínicas como surdez neurossensorial, miopatia, oftalmoplegia externa progressiva, ataxia, neuropatia periférica, acidentes vasculares encefálicos e paraplegia espástica. | |||
| description / en | description / en | ||
Autosomal dominant optic atrophy plus syndrome is a form of autosomal dominant optic atrophy associating optic atrophy with other clinical manifestations such sensorineural deafness, myopathy, progressive external ophthalmoplegia, ataxia, peripheral neuropathy, stroke or spastic paraplegia. | |||
Revision as of 10:16, 16 August 2026
Autosomal dominant optic atrophy plus syndrome is a form of autosomal dominant optic atrophy associating optic atrophy with other clinical manifestations such sensorineural deafness, myopathy, progressive external ophthalmoplegia, ataxia, peripheral neuropathy, stroke or spastic paraplegia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1149710475 |
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| English | Autosomal dominant optic atrophy plus syndrome |
Autosomal dominant optic atrophy plus syndrome is a form of autosomal dominant optic atrophy associating optic atrophy with other clinical manifestations such sensorineural deafness, myopathy, progressive external ophthalmoplegia, ataxia, peripheral neuropathy, stroke or spastic paraplegia. |
