Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Q88314): Difference between revisions
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Displasia congênita espondiloepimetafisária (SEMD), tipo Strudwick é uma forma de SEMD caracterizada por baixa estatura desproporcional desde o nascimento (com um tronco muito curto e membros encurtados) e anormalidades esqueléticas (lordose, escoliose, vértebras achatadas, tórax carinado, coxa vara, pé torto, e epífises ou metáfises anormais). | |||
| description / en | description / en | ||
Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised 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). | |||
Revision as of 14:30, 15 August 2026
Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised 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).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1090803595 |
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| English | Spondyloepimetaphyseal dysplasia congenita, Strudwick type |
Spondyloepimetaphyseal dysplasia congenita (SEMD), Strudwick type is a form of SEMD characterised 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). |
