Disastrous evolution of ollier disease: a rare case report

Ollier disease is a rare genetic disorder characterized by the development of multiple enchondromas. The clinical manifestations of the disease vary widely, but patients often present with bone deformities and an increased risk of developing chondrosarcoma. Here, the authors present a case report of...

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Detalles Bibliográficos
Autores principales: Fadili, Omar, El Khaymy, Khalid, Bouzid, Youssef, El Adaoui, Oussama, El Andaloussi, Yassir, Fadili, Mustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289570/
https://www.ncbi.nlm.nih.gov/pubmed/37363592
http://dx.doi.org/10.1097/MS9.0000000000000678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289570/
https://www.ncbi.nlm.nih.gov/pubmed/37363592
http://dx.doi.org/10.1097/MS9.0000000000000678

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