Late-onset fibrodysplasia ossificans progressiva with atypical presentation: A case report

Fribrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by progressive heterotopic ossification of connective tissues, episodic flare-ups and bilateral deformities of the great toe (hallux valgus). As faulty tissue repair processes progressively calcify tissue, patients...

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Detalles Bibliográficos
Autores principales: Cunningham, Conor M., Royeca, J. Matthew, King, Samuel W., Pandit, Hemant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6664093/
https://www.ncbi.nlm.nih.gov/pubmed/31384566
http://dx.doi.org/10.1016/j.crwh.2019.e00134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6664093/
https://www.ncbi.nlm.nih.gov/pubmed/31384566
http://dx.doi.org/10.1016/j.crwh.2019.e00134

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