Banki syndrome is a synostosis syndrome reported in a single Hungarian family in which members of 3 generations showed lunotriquetral synostosis clinodactyly clinometacarpy brachymetacarpy and leptometacarpy (thin diaphysis). It appeared to be a unique dominant mutation. There have been no further descriptions in the literature since 1965.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2026
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Banki syndrome?
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