Unilateral oculomotor palsy with cerebellar ataxia.
- Specialty
- Neurology
- Subspecialty
- Neurology / Brainstem syndromes
- Sex & age distribution
- Male: affected; Female: affected; Children: rare
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Oculomotor palsy with ataxia
Etiology & mechanism
Lesion of the oculomotor nucleus and superior cerebellar peduncle.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (3)
In plain terms, someone with Nothnagel 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
2 shared
Action myoclonus–renal failure syndrome
ataxia, tremor
1 shared
Abetalipoproteinemia
ataxia
1 shared
Acquired cerebellar syndrome
ataxia
1 shared
Alcohol withdrawal syndrome
tremor
1 shared
Angelman syndrome
ataxia
1 shared
Benedikt syndrome
third nerve palsy
1 shared
Brown–Vialetto–Van Laere syndrome
ataxia
1 shared
Cerebral folate deficiency syndrome
ataxia
1 shared
Claude syndrome
third nerve palsy
1 shared
Dandy–Walker malformation
ataxia
Shares genes with
None.
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