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Myasthenia gravis complicating the surgical management of achondroplasia: a case-based update
BACKGROUND: Achondroplasia is the commonest skeletal dysplasia of autosomal dominant inheritance caused by “gain of function” mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. Foramen magnum compression due to accelerated ossification and spinal canal stenosis secondary to reduced i...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Berlin Heidelberg
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362015/ https://www.ncbi.nlm.nih.gov/pubmed/35908138 http://dx.doi.org/10.1007/s00381-022-05617-1 |