A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly

Eur J Pediatr. 2006 Oct;165(10):734-5. doi: 10.1007/s00431-006-0138-8. Epub 2006 Apr 27.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • DNA-Binding Proteins / genetics*
  • Family Health
  • Headache / etiology
  • Homeodomain Proteins / genetics*
  • Humans
  • Mutation*
  • Parietal Bone / abnormalities*
  • Parietal Bone / diagnostic imaging
  • Pedigree
  • Radiography
  • Skull / blood supply
  • Veins / abnormalities*

Substances

  • DNA-Binding Proteins
  • Homeodomain Proteins
  • MSX2 protein