Branchio-oto-renal syndrome (Q94124): Difference between revisions
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15 August 2026
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Latest 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). |
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CID11:ID_504227287
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dki-india-ID_504227287
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Concluído
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15 August 2026
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