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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...
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| 出版年: | Surg Neurol Int |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Scientific Scholar
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8326084/ https://ncbi.nlm.nih.gov/pubmed/34345494 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.25259/SNI_409_2021 |
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