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...

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Detalles Bibliográficos
Autores principales: Afshari, Fardad T., Parida, Amitav, Debenham, Phillip, Solanki, Guirish A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Case-based Review
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

Internet

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

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