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Up to: Type 2 collagenopathy · Spondyloepimetaphyseal dysplasia · Spondylometaphyseal dysplasia
Spondyloepimetaphyseal dysplasia, Strudwick type
A spondyloepimetaphyseal dysplasia characterized by disproportionate short stature from birth (with a very short trunk and shortened limbs) and skeletal abnormalities (lordosis, scoliosis, flattened vertebrae, pectus carinatum, coxa vara, clubfoot, and abnormal epiphyses or metaphyses).
This condition has no sub-types.