Pediatrics · Pediatrics / Pediatric genetics
Goldenhar syndrome
also: Oculo-auriculo-vertebral spectrum
Hemifacial microsomia with ear, eye and vertebral anomalies.
- Specialty
- Pediatrics
- Subspecialty
- Pediatrics / Pediatric genetics
- Sex & age distribution
- Male: affected, slight male predominance; Female: affected; Children: yes, congenital
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Oculo-auriculo-vertebral spectrum
Etiology & mechanism
First and second branchial arch developmental disruption.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (5)
In plain terms, someone with Goldenhar syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
CHARGE syndrome
ear anomalies, hearing loss
1 shared
Aicardi syndrome
vertebral anomalies
1 shared
Alport syndrome with diffuse leiomyomatosis
hearing loss
1 shared
Alström syndrome
hearing loss
1 shared
Branchio-oto-renal syndrome
hearing loss
1 shared
Chanarin–Dorfman syndrome
hearing loss
1 shared
Cockayne syndrome
hearing loss
1 shared
Cogan syndrome
hearing loss
1 shared
Cogan syndrome with neurological involvement
hearing loss
1 shared
Cornelia de Lange syndrome
hearing loss
Shares genes with
None.
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