Spondyloepimetaphyseal dysplasia

(Redirected from Strudwick syndrome)

Spondyloepimetaphyseal dysplasia is a genetic condition affecting the bones.[1]

Spondyloepimetaphyseal dysplasia
Other namesSpondyloepimetaphyseal dysplasia congenita, Strudwick type
Spondyloepimetaphyseal dysplasia is inherited in an autosomal dominant manner

Types include:

References

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  1. ^ 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.






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