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Ramsay Hunt syndrome type 1: Difference between revisions
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'''Ramsay Hunt syndrome (RHS) type''' 1 is a rare, degenerative, neurological disorder characterized by [[jerk|myoclonus]] epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairmen<ref>https://en.wikipedia.org/wiki/Ramsay_Hunt_syndrome_type_1</ref> | '''Ramsay Hunt syndrome (RHS) type''' 1 is a rare, degenerative, neurological disorder characterized by [[jerk|myoclonus]] epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairmen<ref>https://en.wikipedia.org/wiki/Ramsay_Hunt_syndrome_type_1</ref> | ||
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175171/ Progressive myoclonus ataxia: Time for a new definition?] | |||
{{Wikidata|Q3961686}} | {{Wikidata|Q3961686}} | ||
{{refs}} | {{refs}} |
Latest revision as of 16:42, 8 June 2019
Ramsay Hunt cerebellar syndrome or myoclonic cerebellar dyssynergia
Ramsay Hunt syndrome (RHS) type 1 is a rare, degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairmen[1]
Progressive myoclonus ataxia: Time for a new definition?
References: |