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Fibrodysplasia ossificans progressiva
Fibrodysplasia ossificans progressiva (FOP), a rare and disabling genetic condition of congenital skeletal malformations and progressive heterotopic ossification (HO), is the most catastrophic disorder of HO in humans. Episodic disease flare-ups are precipitated by soft tissue injury, and immobility...
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| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2008
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2424023/ https://ncbi.nlm.nih.gov/pubmed/18328989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.berh.2007.11.007 |
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