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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...
Autores principales: | Shi, Xiaofei, Zhou, Liqing, Shang, Jingjing, Wang, Ke, Chu, Cong-Qiu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
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 |
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