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Disease: Brachymesophalangy type 2

  • Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family
  • Brachydactyly type A4 (brachymesophalangia II and V, Temtamy type). A rare type of brachydactyly
  • Feingold syndrome
  • Feingold syndrome type 2 in a patient from China
  • Free fat graft for congenital hand differences
  • Further delineation of spondyloepimetaphyseal dysplasia Faden-Alkuraya type: A RSPRY1-associated spondylo-epi-metaphyseal dysplasia with cono-brachydactyly and craniosynostosis
  • Laurin-Sandrow syndrome with additional associated manifestations
  • Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger
  • Type A2 brachydactily: report of a new family
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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