Spondyloepimetaphyseal dysplasia
(Redirected from Strudwick syndrome)
| Spondyloepimetaphyseal dysplasia | |
|---|---|
| Other names | Spondyloepimetaphyseal dysplasia congenita, Strudwick type |
 | |
| Spondyloepimetaphyseal dysplasia is inherited in an autosomal dominant manner | |
Spondyloepimetaphyseal dysplasia is a genetic condition affecting the bones.[1]
Types include:
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloepiphyseal dysplasia congenita
- Spondyloepimetaphyseal dysplasia, Pakistani type
References[edit]
- ^ Ian Young (15 June 2002). Genetics for Orthopedic Surgeons: The Molecular Genetic Basis of Orthopedic Disorders. Remedica. pp. 41–. ISBN 978-1-901346-42-8. Retrieved 3 January 2011.
External links[edit]