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Bencze syndrome: A rare inherited condition characterized mainly by abnormal, asymmetrical facial bone growth and eye problems in some cases. More detailed information about the symptoms, causes, and treatments of Bencze 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 Bencze syndrome as a "rare disease".
Source - Orphanet
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