Skip to main content
Journal of Clinical Laboratory Analysis logoLink to Journal of Clinical Laboratory Analysis
. 2006 Feb 8;20(1):23–26. doi: 10.1002/jcla.20096

Mutation analysis of Crouzon syndrome in Taiwanese patients

Chin‐Ping Chang 1,3,, Lei Wan 1,3,5,, Chang‐Hai Tsai 5, Cheng‐Chun Lee 1, Fuu‐Jen Tsai 1,2,3,4,
PMCID: PMC6807587  PMID: 16470531

Abstract

Crouzon syndrome is an autosomal‐dominant disorder that causes premature fusion of the cranial suture. Crouzon, Pfeiffer, and Apert syndromes are caused by mutations in the extracellular, third immunoglobulin‐like domain, and adjacent linker regions (exons IIIa and IIIc) of the fibroblast growth factor receptor 2 (FGFR2) gene. We screened 12 Crouzon syndrome patients for mutations in exons IIIa and IIIc of the FGFR2 gene by polymerase chain reaction (PCR) and direct sequencing. Mutations were detected in nine of 12 patients at amino acid positions 278, 281, 289, 342, and 354. More than half of the studied Crouzon patients carried a mutation resulting in either the loss or gain of a cysteine residue. A novel missense Ser354Phe substitution at exon IIIc of the human FGFR2 gene was found. According to our results, sequencing analysis of IgIII domain of the FGFR2 gene can lead to a genetic diagnosis of Crouzon syndrome. J. Clin. Lab. Anal. 20:23–26, 2006. © 2006 Wiley‐Liss, Inc.

Keywords: Crouzon syndrome, FGFR2 gene, mutation, IgIII

REFERENCES

  • 1. Cohen MM Jr. Craniosynostosis: diagnosis, evaluation and management. New York: Raven Press; 1986. p 480. [Google Scholar]
  • 2. Winter RM, Baraitser M. The Landon dysmorphology database. Oxford: Oxford University Press; 1994. [Google Scholar]
  • 3. Reardon W, Winter RM, Rutland P, Pulleyn LJ, Jones BM, Malcolm S. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nat Genet 1994;8:98–103. [DOI] [PubMed] [Google Scholar]
  • 4. Park WJ, Meyers GA, Li X, et al. Novel FGFR2 mutations in Crouzon and Jackson‐Weiss syndromes show allelic heterogeneity and phenotypic variability. Hum Mol Genet 1995;4:1229–1233. [DOI] [PubMed] [Google Scholar]
  • 5. Steinberger D, Mulliken JB, Müller U. Predisposition for cysteine substitution in the immunoglobulin‐like chain of FGFR2 in Crouzon syndrome. Hum Genet 1995;96:113–115. [DOI] [PubMed] [Google Scholar]
  • 6. Tsai FJ, Yang CF, Wu JU, Tsai CH, Lee CC. Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients. Pediatr Int 2001;43:263–266. [DOI] [PubMed] [Google Scholar]
  • 7. Park WJ, Theda C, Maestri NE, et al. Analysis of phenotypic features and FGFR2 mutations in Apert syndrome. Am J Hum Genet 1995;57:321–328. [PMC free article] [PubMed] [Google Scholar]
  • 8. Wilkie AO, Slaney SF, Oldridge M, et al. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 1995;9:165–172. [DOI] [PubMed] [Google Scholar]
  • 9. Muenke M, Schell U, Hehr A, et al. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome. Nat Genet 1994;8:269–274. [DOI] [PubMed] [Google Scholar]
  • 10. Rutland P, Pulleyn LJ, Reardon W, et al. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Nat Genet 1995;9:173–176. [DOI] [PubMed] [Google Scholar]
  • 11. Jabs EW, Li X, Scott AF, et al. Jackson‐Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nat Genet 1994;8:275–279. [DOI] [PubMed] [Google Scholar]
  • 12. Oldridge M, Wilkie AO, Slaney SF, et al. Mutation in the third immunoglobulin domain of the fibroblast growth factor receptor‐2 gene in Crouzon syndrome. Hum Mol Genet 1995;4:1077–1082. [DOI] [PubMed] [Google Scholar]
  • 13. Fujisawa H, Hasegawa M, Kida S, Yamashita J. A novel fibroblast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia. J Neurosurg 2002;97:396–400. [DOI] [PubMed] [Google Scholar]
  • 14. Weidemann HR, Kunze J. Clinical syndrome: Crouzon syndrome. London: Times Mirror International Publishers Limited; 1995. p 12–13. [Google Scholar]
  • 15. Abou‐Sleiman PM, Apessos A, Harper JC, Serhal P, Delhanty JD. Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome. Mol Hum Reprod 2002;8:304–309. [DOI] [PubMed] [Google Scholar]
  • 16. Mulliken JB, Steinberger D, Kunze S, Muller U. Molecular diagnosis of bilateral coronal synostosis. Plast Reconstr Surg 1999;104:1603–1615. [DOI] [PubMed] [Google Scholar]
  • 17. Passos‐Bueno MR, Wilcox WR, Jabs EW, Sertie AL, Alonso LG, Kitoh H. Clinical spectrum of fibroblast growth factor receptor mutations. Hum Mutat 1999;14:115–125. [DOI] [PubMed] [Google Scholar]
  • 18. Steinberger D, Vriend G, Mulliken JB, Miller U. The mutation in FGFR2‐ associated craniosynostoses are clustered in five structural elements of immunoglobulin‐like domain III of receptor. Hum Genet 1998;102:145–150. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Laboratory Analysis are provided here courtesy of Wiley

RESOURCES