Usher syndrome (Q46732): Difference between revisions
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Síndrome de Usher é a causa mais comum de surdez-cegueira hereditária combinada e é caracterizada pela associação de surdez neurossensorial (geralmente congênita) com retinite pigmentosa e perda progressiva da visão. | |||
| description / en | description / en | ||
Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss. | |||
Revision as of 15:31, 13 August 2026
Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD2H.4 |
||
| English | Usher syndrome |
Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss. |
