Article
Craniosynostosis: novel insights into pathogenesis and treatment.
Current opinion in neurology - 1 Apr 1996
Wilkie A O, Wall S A
Abstract excerpt
The identification in craniosynostosis syndromes of mutations in genes belonging to the fibroblast growth factor signalling pathway and the transcriptional regulator MSX2 provides important clues to the pathogenesis of these disorders. Although surgery continues to be the mainstay of treatment, n...
Topics
- Acrocephalosyndactylia
- Craniosynostoses
- Humans
- Mutation
- Receptors, Nerve Growth Factor
