Bilateral corticobulbar damage.
- Specialty
- Neurology
- Subspecialty
- Neurology / Behavioral neurology
- Sex & age distribution
- Male: affected; Female: affected; Children: rare
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Pseudobulbar syndrome
Etiology & mechanism
Bilateral upper motor neuron lesions.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (3)
In plain terms, someone with Pseudobulbar palsy 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.
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Shares symptoms with
2 shared
Foix–Chavany–Marie syndrome
dysarthria, dysphagia
2 shared
Osmotic demyelination syndrome
dysarthria, dysphagia
2 shared
Progressive supranuclear palsy
dysarthria, dysphagia
1 shared
Acquired cerebellar syndrome
dysarthria
1 shared
Alport syndrome with diffuse leiomyomatosis
dysphagia
1 shared
Avellis syndrome
dysphagia
1 shared
Brainstem stroke syndrome
dysarthria
1 shared
Collet–Sicard syndrome
dysphagia
1 shared
Eagle syndrome
dysphagia
1 shared
Facial-onset sensory and motor neuronopathy
dysphagia
Shares genes with
None.
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