Branchio-oto-renal syndrome (Q94124): Difference between revisions
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Síndrome brânquio-oto-renal (BOR) é caracterizada por anomalias do arco branquial (fendas branquiais, fístulas, cistos), deficiência auditiva (malformações da aurícula com fossas pré-auriculares, deficiência auditiva condutiva ou neurossensorial) e malformações renais (malformação da árvore urinária, hipoplasia renal ou agenesia, displasia renal, cistos renais). | |||
| description / en | description / en | ||
Branchiootorenal (BOR) syndrome is characterised by branchial arch anomalies (branchial clefts, fistulae, cysts), hearing impairment (malformations of the auricle with pre-auricular pits, conductive or sensorineural hearing impairment), and renal malformations (urinary tree malformation, renal hypoplasia or agenesis, renal dysplasia, renal cysts). | |||
Revision as of 09:14, 16 August 2026
Branchiootorenal (BOR) syndrome is characterised by branchial arch anomalies (branchial clefts, fistulae, cysts), hearing impairment (malformations of the auricle with pre-auricular pits, conductive or sensorineural hearing impairment), and renal malformations (urinary tree malformation, renal hypoplasia or agenesis, renal dysplasia, renal cysts).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_504227287 |
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| English | Branchio-oto-renal syndrome |
Branchiootorenal (BOR) syndrome is characterised by branchial arch anomalies (branchial clefts, fistulae, cysts), hearing impairment (malformations of the auricle with pre-auricular pits, conductive or sensorineural hearing impairment), and renal malformations (urinary tree malformation, renal hypoplasia or agenesis, renal dysplasia, renal cysts). |
