Trigonocephaly in Muenke syndrome

Am J Med Genet A. 2006 Nov 15;140(22):2493-4. doi: 10.1002/ajmg.a.31460.

Abstract

Saethre-Chotzen syndrome is caused by mutations in the TWIST gene on chromosome 7p21.2. However, Muenke et al. [(1997); Am J Hum Genet 91: 555-564] described a new subgroup carrying the Pro250Arg mutation in the fibroblast growth factor receptor (FGFR) 3 gene on chromosome 4p16. Uni or bicoronal synostosis appears to be the main clinical finding in both syndromes. We observed trigonocephaly as a new manifestation in Muenke syndrome. As a consequence we advise to routinely perform mutation analysis of the FGFR1, 2, and 3 genes in children with non-syndromic trigonocephaly.

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Substitution
  • Craniosynostoses / diagnostic imaging
  • Craniosynostoses / genetics*
  • Humans
  • Imaging, Three-Dimensional
  • Infant
  • Male
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics
  • Skull / abnormalities
  • Skull / diagnostic imaging
  • Syndrome
  • Tomography, X-Ray Computed

Substances

  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3