Ataxia spastic congenital miosis: A rare, dominantly inherited disorder characterized mainly by ataxia, spasticity and small pupils that respond poorly to light. More detailed information about the symptoms, causes, and treatments of Ataxia spastic congenital miosis is available below.
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Ataxia spastic congenital miosis as a "rare disease".
Source - Orphanet
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