Pendred syndrome (Q39758): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Síndrome de Pendred é caracterizada pela associação de surdez neurossensorial congênita bilateral, bócio tireoidiano, malformação cócleo-vestibular e potencial disfunção vestibular. | |||
| description / en | description / en | ||
Pendred syndrome is characterised by the association of congenital bilateral neurosensory deafness, thyroid goitre, cochleovestibular malformation and potential vestibular dysfunction. | |||
Revision as of 05:17, 13 August 2026
Pendred syndrome is characterised by the association of congenital bilateral neurosensory deafness, thyroid goitre, cochleovestibular malformation and potential vestibular dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5A00.02 |
||
| English | Pendred syndrome |
Pendred syndrome is characterised by the association of congenital bilateral neurosensory deafness, thyroid goitre, cochleovestibular malformation and potential vestibular dysfunction. |
