Fibroplasia Ossificans Progressiva: A Case Report of a Rare Disease Entity

BACKGROUND: Fibrodysplasia ossificans progressiva (FOP), also known as Myositis ossificans progressiva or Munchmeyer's disease, is an extremely rare and disabling genetic condition of congenital skeletal malformations and progressive heterotopic ossification (HO). The disease is characterized b...

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Detalles Bibliográficos
Autores principales: Solomon, Daniel, Wakjira, Iyasu, Hailu, Daniel, Gorfy, Yocabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Publications Office of Jimma University 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308737/
https://www.ncbi.nlm.nih.gov/pubmed/30607064
http://dx.doi.org/10.4314/ejhs.v28i4.17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308737/
https://www.ncbi.nlm.nih.gov/pubmed/30607064
http://dx.doi.org/10.4314/ejhs.v28i4.17

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