Branchio-oculo-facial syndrome (Q94130): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 09:14, 16 August 2026
Branchio-oculo-facial syndrome (BOFS) is a genetic syndrome characterised by low birth weight and growth retardation, bilateral branchial clefts that may be hemangiomatous, sometimes with linear skin lesions behind the ears ('burn-like' lesions), congenital strabismus, obstructed nasolacrimal ducts, a broad nasal bridge with a flattened nasal tip, a protruding upper lip with an unusually broad and prominent philtrum, and full mouth.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1471530044 |
||
| English | Branchio-oculo-facial syndrome |
Branchio-oculo-facial syndrome (BOFS) is a genetic syndrome characterised by low birth weight and growth retardation, bilateral branchial clefts that may be hemangiomatous, sometimes with linear skin lesions behind the ears ('burn-like' lesions), congenital strabismus, obstructed nasolacrimal ducts, a broad nasal bridge with a flattened nasal tip, a protruding upper lip with an unusually broad and prominent philtrum, and full mouth. |
Statements
CID11:ID_1471530044
0 references
dki-india-ID_1471530044
0 references
Concluído
0 references
15 August 2026
0 references
