Banki syndrome
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Summary
A single Hungarian family has been reported in 1965 in the literature in which members of 3 generations showed lunotriquetral synostosis, clinodactyly, clinometacarpy, brachymetacarpy and leptometacarpy (thin diaphysis). It seems to be a unique dominant mutation. *Author : Orphanet (January 2004).*
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