Neurology · Neurology / Movement disorders (ataxias)
Acquired cerebellar syndrome
also: Acquired cerebellar ataxia
Descriptor for ataxia from non-genetic causes.
- Specialty
- Neurology
- Subspecialty
- Neurology / Movement disorders (ataxias)
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, post-infectious cerebellitis in children
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Acquired cerebellar ataxia
- Note
- Umbrella term
Etiology & mechanism
Toxic, immune, vascular, paraneoplastic, infectious.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (3)
In plain terms, someone with Acquired cerebellar 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.
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Shares symptoms with
3 shared
Paraneoplastic cerebellar degeneration syndrome
ataxia, dysarthria, nystagmus
1 shared
Abetalipoproteinemia
ataxia
1 shared
Action myoclonus–renal failure syndrome
ataxia
1 shared
Alström syndrome
nystagmus
1 shared
Angelman syndrome
ataxia
1 shared
Aniridia-Wilms tumor-genitourinary anomalies-retardation syndrome
nystagmus
1 shared
Brainstem stroke syndrome
dysarthria
1 shared
Brown–Vialetto–Van Laere syndrome
ataxia
1 shared
Cerebral folate deficiency syndrome
ataxia
1 shared
Dandy–Walker malformation
ataxia
Shares genes with
None.
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