A rare neurodegenerative disease. Adult patients suffer symptoms such as ataxia, choreoathetosis myoclonus, epilepsy and dementia and children suffer ataxia, myoclonus, epilepsy and mental retardation. The condition is also known as Haw River syndrome or Natito-Oyanagi disease. ...more »
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Dentatorubral Pallidoluysian Atrophy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Dentatorubral Pallidoluysian Atrophy, or a subtype of Dentatorubral Pallidoluysian Atrophy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Dentatorubral Pallidoluysian Atrophy as a "rare disease".
Source - Orphanet
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