Disease aggravation following surgery in a rare patient suspected to Fibrodysplasia (Myositis) ossificans progressiva: a case report

BACKGROUND: Fibrodysplasia ossificans progressiva (FOP) as a rare and heritable disorder with the infrequent genetic transmission of the condition is a catastrophic disorder of heterotopic ossification (HO) and a cause of extraskeletal bone formation in humans. Given the lack of effective treatment...

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Detalles Bibliográficos
Autores principales: Zarei, Amir, Rahimi, Foad, Khadem, Mehryar, Moradi, Mansour, Rahmani, Khaled
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694942/
https://www.ncbi.nlm.nih.gov/pubmed/38044456
http://dx.doi.org/10.1186/s13256-023-04253-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694942/
https://www.ncbi.nlm.nih.gov/pubmed/38044456
http://dx.doi.org/10.1186/s13256-023-04253-w

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