Buttiens-Fryns syndrome: A rare genetic disorder characterized by a small jaw, small mouth and defects involving the hands and feet. More detailed information about the symptoms, causes, and treatments of Buttiens-Fryns syndrome is available below.
See full list of 13 symptoms of Buttiens-Fryns syndrome
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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 Buttiens-Fryns syndrome as a "rare disease".
Source - Orphanet
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