Ventricular septal defect in Crouzon Syndrome: case report

Genet Couns. 2012;23(4):519-22.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Craniofacial Dysostosis / diagnosis
  • Craniofacial Dysostosis / genetics*
  • Developmental Disabilities / genetics
  • Facies
  • Female
  • Heart Septal Defects, Ventricular / diagnosis
  • Heart Septal Defects, Ventricular / genetics*
  • Humans
  • Intellectual Disability / genetics
  • Middle Aged
  • Mutation / genetics*
  • Receptor, Fibroblast Growth Factor, Type 2 / genetics*
  • Turkey
  • Ultrasonography
  • Ventricular Septum / diagnostic imaging

Substances

  • FGFR2 protein, human
  • Receptor, Fibroblast Growth Factor, Type 2