Neurology · Neurology / Neuromuscular
Facial-onset sensory and motor neuronopathy
also: FOSMN; Vucic–Kiernan syndrome
Sporadic neuronopathy starting on the face.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neuromuscular
- Sex & age distribution
- Male: affected, slight male predominance; Female: affected; Children: no, adult onset
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- FOSMN; Vucic–Kiernan syndrome
Etiology & mechanism
TDP-43 pathology.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (5)
In plain terms, someone with Facial-onset sensory and motor neuronopathy 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
1 shared
Alport syndrome with diffuse leiomyomatosis
dysphagia
1 shared
Avellis syndrome
dysphagia
1 shared
Collet–Sicard syndrome
dysphagia
1 shared
Eagle syndrome
dysphagia
1 shared
Foix–Chavany–Marie syndrome
dysphagia
1 shared
Guillain–Barré syndrome, pharyngeal-cervical-brachial variant
bulbar weakness
1 shared
Hereditary diffuse gastric cancer syndrome
dysphagia
1 shared
Jackson syndrome
dysphagia
1 shared
Opalski syndrome
dysphagia
1 shared
Osmotic demyelination syndrome
dysphagia
Shares genes with
None.
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