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Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
RATIONALE: Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder characterized by congenital skeletal deformities and soft tissue masses that progress into heterotopic ossification. Deformities of the great toes are distinctive and heterotrophic ossification usually begin...
Autores principales: | Wang, Zhankui, Wang, Xiuhua, Liu, Baojin, Hou, Yanfeng |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7939192/ https://www.ncbi.nlm.nih.gov/pubmed/33655926 http://dx.doi.org/10.1097/MD.0000000000024620 |
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