Long QT syndrome with hearing impairment (Q66175): Difference between revisions
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A síndrome de Jervell e Lange-Nielsen é uma variante autossômica recessiva da síndrome do QT longo familiar, caracterizada por perda auditiva neurossensorial profunda bilateral congênita, um intervalo QT longo no eletrocardiograma e taquiarritmias ventriculares. | |||
| description / en | description / en | ||
Jervell and Lange-Nielsen syndrome is an autosomal recessive variant of familial long QT syndrome characterised by congenital profound bilateral sensorineural hearing loss, a long QT interval on electrocardiogram and ventricular tachyarrhythmias. | |||
Revision as of 13:58, 14 August 2026
Jervell and Lange-Nielsen syndrome is an autosomal recessive variant of familial long QT syndrome characterised by congenital profound bilateral sensorineural hearing loss, a long QT interval on electrocardiogram and ventricular tachyarrhythmias.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1346057986 |
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| English | Long QT syndrome with hearing impairment |
Jervell and Lange-Nielsen syndrome is an autosomal recessive variant of familial long QT syndrome characterised by congenital profound bilateral sensorineural hearing loss, a long QT interval on electrocardiogram and ventricular tachyarrhythmias. |
