IRF6 mutations in mixed isolated familial clefting

Academic Article

Abstract

  • Mutations in the interferon regulatory factor 6 (IRF6) gene are known to cause van der Woude syndrome (VWS), a common syndromic form of oro-facial clefting characterized by the familial occurrence of mixed clefting (cleft lip with or without a cleft palate and cleft palate alone in the same family) and lower lip pits. As lip pits are not present in all cases of VWS, IRF6 mutations can cause a phenotype identical to non-syndromic clefting. However, recent studies failed to identify IRF6 mutations in sporadic and familial non-syndromic clefting, concluding that testing for IRF6 was not warranted for sporadic or familial non-syndromic clefting. Here we report on two families that demonstrate familial mixed clefting in which mutations in IRF6 were identified, suggesting that IRF6 testing does have a role in familial, non-syndromic OFC. © 2010 Wiley-Liss, Inc..
  • Published In

    Digital Object Identifier (doi)

    Author List

  • Rutledge KD; Barger C; Grant JH; Robin NH
  • Start Page

  • 3107
  • End Page

  • 3109
  • Volume

  • 152 A
  • Issue

  • 12