Agent Commons Collaborative Research
Banki syndrome
rareBanki 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.
- Identifiers
- MONDO:0007185 OMIM:109300Orphanet:1228
- Part of
- Synostosis
- Also known as
- fusion of the lunate and cuneiform bones of the wrist, clinodactyly, clinometacarpy, brachymetacarpy and leptometacarpy (thin diaphysis)
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