Spondyloepimetaphyseal dysplasia
| 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
Variant of SMD type A4-a)Metaphyseal involvement of the distal radius and ulna b)metaphyseal involvement and severe coxa valga c) lumbar lordosis d) spinal scoliosis in spite of 6 years of bracing e) delayed ossification of pubic bones f) severe metaphyseal changes and genu valgum deformity g)severe metaphyseal involvement of forearm bones
References
- ↑ 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. Archived from the original on 8 February 2022. Retrieved 3 January 2011.
External links
| Classification | |
|---|---|
| External resources |
|
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.