Spondyloepimetaphyseal dysplasia, Strudwick type Other Information |
Dappled metaphysis syndrome; SED Strudwick; SEMD, Strudwick type; SMED, Strudwick type; SMED, type I; Spondylometaepiphyseal dysplasia congenita, Strudwick type; Spondylometaphyseal dysplasia (SMD); Spondylometaphyseal Dysplasia, Strudwick Type; Strudwick syndrome |
Spondyloepimetaphyseal dysplasia, Strudwick type is an inherited disorder of bone growth that results in dwarfism, characteristic skeletal abnormalities, and problems with vision. The name of the condition indicates that it affects the bones of the spine (spondylo-) and two regions near the ends of bones (epiphyses and metaphyses). The type was named after the first reported patient with the disorder. Spondyloepimetaphyseal dysplasia, Strudwick type is a subtype of collagenopathy, types II a ...
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Spondyloepimetaphyseal dysplasia, Strudwick type
... Spondyloepimetaphyseal dysplasia, Strudwick type is an inherited disorder of bone growth that results in short stature (dwarfism), characteristic skeletal abnormalities, and problems with vision. The ...
Source: Genetics Home Reference
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