Neurology · Neurology / Ataxias
Ramsay Hunt syndrome type 1
also: Dyssynergia cerebellaris myoclonica
Progressive myoclonus with cerebellar ataxia.
- Specialty
- Neurology
- Subspecialty
- Neurology / Ataxias
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- EPM1A, MT-TK
- Alternative names & eponyms
- Dyssynergia cerebellaris myoclonica
Etiology & mechanism
Mitochondrial or storage disorder.
Gene(s) involved (2)
Symptoms & signs (4)
In plain terms, someone with Ramsay Hunt syndrome type 1 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
Action myoclonus–renal failure syndrome
action myoclonus, ataxia, seizures
2 shared
Angelman syndrome
ataxia, seizures
2 shared
Cerebral folate deficiency syndrome
ataxia, seizures
2 shared
EAST syndrome
ataxia, seizures
2 shared
MELAS syndrome
cognitive decline, seizures
2 shared
NARP syndrome
ataxia, seizures
1 shared
Abetalipoproteinemia
ataxia
1 shared
Acquired cerebellar syndrome
ataxia
1 shared
Alcohol withdrawal syndrome
seizures
1 shared
Amniotic fluid embolism syndrome
seizures
Shares genes with
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