Neurology · Neurology / Cranial nerve syndromes
Collet–Sicard syndrome
also: Condylar-jugular foramen syndrome
Palsy of cranial nerves IX, X, XI and XII.
- Specialty
- Neurology
- Subspecialty
- Neurology / Cranial nerve syndromes
- Sex & age distribution
- Male: affected; Female: affected; Children: rare
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Condylar-jugular foramen syndrome
Etiology & mechanism
Retroparotid or skull base lesion.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (4)
In plain terms, someone with Collet–Sicard 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
3 shared
Jackson syndrome
dysphagia, hoarseness, shoulder weakness
2 shared
Avellis syndrome
dysphagia, hoarseness
2 shared
Tapia syndrome
dysphagia, hoarseness
2 shared
Vernet syndrome
dysphagia, hoarseness
2 shared
Villaret syndrome
dysphagia, hoarseness
1 shared
Alport syndrome with diffuse leiomyomatosis
dysphagia
1 shared
Eagle syndrome
dysphagia
1 shared
Facial-onset sensory and motor neuronopathy
dysphagia
1 shared
Foix–Chavany–Marie syndrome
dysphagia
1 shared
Hereditary diffuse gastric cancer syndrome
dysphagia
Shares genes with
None.
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