Gunal-Seber-Basaran syndrome: A rare syndrome characterized by dactyocystitis (tear duct infection) and osteopoikilosis (hardened areas on ends of bones). More detailed information about the symptoms, causes, and treatments of Gunal-Seber-Basaran syndrome 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 Gunal-Seber-Basaran syndrome as a "rare disease".
Source - Orphanet
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