Neuronal intranuclear inclusion disease: A very rare syndrome characterized mainly by muscle and nerve degeneration. More detailed information about the symptoms, causes, and treatments of Neuronal intranuclear inclusion disease is available below.
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Prognosis for Neuronal intranuclear inclusion disease: progresses slowly over 1 or 2 decades and leads to death
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Neuronal intranuclear inclusion disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Neuronal intranuclear inclusion disease, or a subtype of Neuronal intranuclear inclusion disease,
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 Neuronal intranuclear inclusion disease as a "rare disease".
Source - Orphanet
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