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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2015
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| 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 |