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Achondroplasia with seronegative spondyloarthropathy resulting in recurrent spinal stenosis : A case report
BACKGROUND: Achondroplasia is an autosomal dominant condition caused by the G380 mutation of the gene encoding fibroblast growth factor receptor 3 on chromosome 4P. The classical findings include rhizomelic extremities, short stature, and spinal stenosis involving the upper cervical and distal lumba...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Scientific Scholar
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326084/ https://www.ncbi.nlm.nih.gov/pubmed/34345494 http://dx.doi.org/10.25259/SNI_409_2021 |