PROGRESSIVE OSSIFYING FIBRODYSPLASIA: CASE REPORT

Progressive ossifying fibrodysplasia is a rare genetic disease that affects one individual in every two million births. Its main consequence is heterotopic ossification, i.e. formation of additional bone in abnormal locations. It is an autosomal dominant disease, usually caused by a new mutation in...

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Detalles Bibliográficos
Autores principales: Romani, Fabiana, de Menezes Karam, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799342/
https://www.ncbi.nlm.nih.gov/pubmed/27047836
http://dx.doi.org/10.1016/S2255-4971(15)30335-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799342/
https://www.ncbi.nlm.nih.gov/pubmed/27047836
http://dx.doi.org/10.1016/S2255-4971(15)30335-9

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