Camurati–Engelmann Disease: A Case-Based Review About an Ultrarare Bone Dysplasia

Camurati–Engelmann disease or progressive diaphyseal dysplasia is a rare hereditary disease that results in a symmetrical hyperostosis of the long bones (cortical thickening) and/or the base of the skull. Camurati–Engelmann disease is also associated with myopathy and neurological manifestations. Cl...

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Detalles Bibliográficos
Autores principales: Klemm, Philipp, Aykara, Iris, Lange, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mesut Onat 2023
Materias:
Case-Based Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152113/
https://www.ncbi.nlm.nih.gov/pubmed/36880809
http://dx.doi.org/10.5152/eurjrheum.2023.21115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152113/
https://www.ncbi.nlm.nih.gov/pubmed/36880809
http://dx.doi.org/10.5152/eurjrheum.2023.21115

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