Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

G. A. Bellus, K. Gaudenz, E. H. Zackai, L. A. Clarke, J. Szabo, C. A. Francomano, M. Muenke

Research output: Contribution to journalArticle


Pfeiffer syndrome (PS; McKusick MIM 101600) is an autosomal dominant craniosynostosis syndrome with characteristic craniofacial anomalies and broad thumbs and big toes. We have previously demonstrated genetic heterogeneity in PS and mapped a gene to chromosome 8 (ref. 3) and a second to chromosome 10 (ref. 4). The gene on chromosome 8 is the fibroblast growth factor receptor 1 (FGFR1) with a common mutation (C755G) predicting a Pro252Arg substitution. The gene on chromosome 10 is FGFR2 with several different mutations causing sporadic and familial PS (Table 1). We report a recurrent single point mutation in the FGFR3 gene, located on chromosome 4p, in ten unrelated families with craniosynostosis syndromes. This mutation (C749G) predicts a Pro250Arg amino acid substitution in the extracellular domain of the FGFR3 protein. Interestingly, this common mutation occurs precisely at the analogous position within the FGFR3 protein as the mutations in FGFR1 (Pro252Arg) and FGFR2 (Pro253Arg) previously reported in Pfeiffer and Apert syndromes, respectively.

Original languageEnglish (US)
Pages (from-to)174-176
Number of pages3
JournalNature genetics
Issue number2
StatePublished - Oct 21 1996
Externally publishedYes


ASJC Scopus subject areas

  • Genetics

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