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...

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Detalles Bibliográficos
Autores principales: Wang, Zhankui, Wang, Xiuhua, Liu, Baojin, Hou, Yanfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
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

Internet

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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