Ramsay Hunt syndrome type 1
Script error: No such module "other uses". Template:Infobox medical condition (new) Ramsay Hunt syndrome type 1 is a rare, degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment [1]
It has also been alternatively called Script error: No such module "Lang".,[2][3] dyssynergia cerebellaris progressiva,[4] dentatorubral degeneration, or Ramsay Hunt cerebellar syndrome.
Presentation
Onset of symptoms usually occurs in early adulthood and is characterized by intention tremor, progressive ataxia, convulsions, and myoclonic epileptic jerks.[1] Tremors usually affect one extremity, primarily the upper limb, and eventually involve the entire voluntary motor system.[1] Overall, the lower extremity is usually disturbed less often than the upper extremity.[1] Additional features of the syndrome include: an unsteady gait, seizures, muscular hypotonia, reduced muscular coordination, asthenia, adiadochokinesia and errors with estimating range, direction, and force of voluntary movements.[1] Mental deterioration can, rarely, occur.[1]
Causes
Ramsay Hunt syndrome type 1 is caused by the impairment of a regulatory mechanism between cerebellar and brainstem nuclei and has been associated with a wide range of diseases, including Lafora disease, dentatorubropallidoluysian atrophy, and celiac disease.[5][6]
Diagnosis
The diagnosis of Ramsay Hunt syndrome type 1 is different to individual people with the syndrome.
Treatment
Treatment of Ramsay Hunt syndrome type 1 is specific to individual symptoms.[1] Myoclonus and seizures may be treated with drugs like valproate.[1] Some have described this condition as difficult to characterize.[7]
Eponym
It is named for James Ramsay Hunt,[8] who first described a form of progressive cerebellar dyssynergia associated with myoclonic epilepsy in 1921.[1]
References
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- ↑ synd/2245 at Whonamedit?
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