Spondyloepimetaphyseal dysplasia
(Redirected from Strudwick syndrome)
Spondyloepimetaphyseal dysplasia | |
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Other names: Spondyloepimetaphyseal dysplasia congenita, Strudwick type | |
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Spondyloepimetaphyseal dysplasia is inherited in an autosomal dominant manner | |
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Spondyloepimetaphyseal dysplasia is a genetic condition affecting the bones.[1]
Types include:
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloepiphyseal dysplasia congenita
- Spondyloepimetaphyseal dysplasia, Pakistani type
![](https://nccommons.org/media/thumb/0/09/PMC3402664_13353_2012_94_Fig3_HTML.png/350px-PMC3402664_13353_2012_94_Fig3_HTML.png)
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.
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Classification | |
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