Branchio-oto-renal syndrome (Q94124): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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 |
||
| 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). |
Statements
CID11:ID_504227287
0 references
dki-india-ID_504227287
0 references
Concluído
0 references
