Fibrodysplasia ossificans progressiva—a rare disease with distinctive features yet still a diagnostic challenge: A case report

RATIONALE: Fibrodysplasia ossificans progressiva (FOP) is rare genetic disease featuring progressive heterotopic ossification of soft tissues of the musculoskeletal system which leads to severe disability and premature death. Recognition of this disease is important since invasive diagnostic procedu...

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Detalles Bibliográficos
Autores principales: Shi, Xiaofei, Zhou, Liqing, Shang, Jingjing, Wang, Ke, Chu, Cong-Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
6900
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440274/
https://www.ncbi.nlm.nih.gov/pubmed/32332674
http://dx.doi.org/10.1097/MD.0000000000019933

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440274/
https://www.ncbi.nlm.nih.gov/pubmed/32332674
http://dx.doi.org/10.1097/MD.0000000000019933

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