Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Q88314): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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). |
Statements
CID11:ID_1090803595
0 references
dki-india-ID_1090803595
0 references
Concluído
0 references
13 August 2026
0 references
