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). | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/504227287 / rank | |||||||||||||||
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CID11:ID_504227287 | |||||||||||||||
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dki-india-ID_504227287 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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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 |
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| 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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