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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Mesut Onat
2023
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| Materias: | |
| 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 |