Muenke syndrome with osteochondroma

Am J Med Genet A. 2009 Feb;149A(2):260-1. doi: 10.1002/ajmg.a.32616.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Face / abnormalities
  • Foot Bones / abnormalities
  • Growth Disorders / genetics
  • Hearing Loss / genetics
  • Humans
  • Male
  • Osteochondroma / etiology
  • Osteochondroma / genetics*
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics*
  • Syndrome
  • Synostosis / genetics

Substances

  • Receptor, Fibroblast Growth Factor, Type 3