Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene

John M. Graham, Stephen R. Braddock, Geert R. Mortier, Ralph Lachman, Cornelis Van Dop, Ethylin Wang Jabs

Research output: Contribution to journalArticle

Abstract

Recently, a unique Pro250Arg point mutation in fibroblast growth factor receptor 3 (FGFR3) was reported in 61 individuals with coronal craniosynostosis from 20 unrelated families [Muenke et al. (1997): Am J Hum Genet 60:555-564]. The discovery of this apparently common mutation has resulted in the definition of a recognizable syndrome, through analysis of subtle clinical findings in families who were previously thought to have a variety of other craniosynostosis syndromes. Previous diagnoses in some of these families have included Jackson-Weiss, Saethre-Chotzen, and Pfeiffer syndromes, as well as Adelaide-type craniosynostosis and brachydactyly- craniosynostosis syndrome [Ades et al. (1994): Am J Med Genet 51:121-130; von Gernet et al. (1996): Am J Med Genet 63:177-184; Reardon et al. (1997): J Med Genet 34:632636; Bellus et al. (1996): Nat Genet 14:174176; Hollaway et al. (1995): Hum Mol Genet 4:681-683; Glass et al. (1994): Clin Dysmorphol 3:215- 223]. There appears to be a need to further delineate the phenotype associated with this common mutation in FGFR3. We compare the clinical characteristics of previously reported cases of this Unique Pro250Arg mutation with those of two additional families and suggest that this syndrome with a unique mutational basis be designated coronal craniosynostosis with brachydactyly and carpal]tarsal coalition due to Pro250Arg mutation in FGFR3 gene, to emphasize the distinctive findings which may be present even in the absence of coronal craniosynostosis.

Original languageEnglish (US)
Pages (from-to)322-329
Number of pages8
JournalAmerican Journal of Medical Genetics
Volume77
Issue number4
DOIs
StatePublished - May 26 1998

Fingerprint

Receptor, Fibroblast Growth Factor, Type 3
Brachydactyly
Viverridae
Craniosynostoses
Wrist
Mutation
Acrocephalosyndactylia
Genes
Point Mutation
Glass
Muenke Syndrome
Tarsal Coalition
Phenotype

Keywords

  • Brachydactyly
  • Carpal coalition
  • Coronal craniosynostosis
  • Fibroblast growth factor receptor 3 (FGFR3)
  • Tarsal coalition

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene. / Graham, John M.; Braddock, Stephen R.; Mortier, Geert R.; Lachman, Ralph; Van Dop, Cornelis; Jabs, Ethylin Wang.

In: American Journal of Medical Genetics, Vol. 77, No. 4, 26.05.1998, p. 322-329.

Research output: Contribution to journalArticle

Graham, John M. ; Braddock, Stephen R. ; Mortier, Geert R. ; Lachman, Ralph ; Van Dop, Cornelis ; Jabs, Ethylin Wang. / Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene. In: American Journal of Medical Genetics. 1998 ; Vol. 77, No. 4. pp. 322-329.
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AU - Van Dop, Cornelis

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