Medicine:Spondyloepimetaphyseal dysplasia
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Revision as of 16:51, 11 August 2021 by imported>MainAI6 (update)
Spondyloepimetaphyseal dysplasia | |
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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
- ↑ 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. https://books.google.com/books?id=QyVsI5b2zJoC&pg=PT41. Retrieved 3 January 2011.
External links
Classification | |
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External resources |
Original source: https://en.wikipedia.org/wiki/Spondyloepimetaphyseal dysplasia.
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