Anderson, P.J.Snell, B.Moore, M.H.2015-05-282015-05-282013Journal of Craniofacial Surgery, 2013; 24(4):1484-14851536-37321536-3732http://hdl.handle.net/2440/91461Muencke syndrome results from mutations in the FGFR3 gene, and although it is well recognized that the clinical presentation is variable, the important key finding includes coronal synostosis. We present a family where a mother with proven FGFR3 Pro250Arg mutation gave birth to identical twins both of whom had craniosynostosis but had coexisting bilateral cleft lip and palate. We believe that this is the first description of clefting occurring in conjunction with Muencke syndrome and so further extends the range of phenotypic variation that can occur in this syndrome.en© 2013 Mutaz B. Habal, MDHumansCraniosynostosesCleft PalateCleft LipSyndromeDiseases in TwinsUltrasonography, PrenatalDNA Mutational AnalysisTwins, MonozygoticAdultInfantInfant, NewbornFemaleMaleReceptor, Fibroblast Growth Factor, Type 3Journal article003002283410.1097/SCS.0b013e31829035c30003301290001582-s2.0-84880873663108414Anderson, P.J. [0000-0002-3730-4652]Moore, M.H. [0000-0003-2136-0315]