AB1029 FIBRODYSPLASIA OSSIFICANS PROGRESSIVA: A CHALLENGE TO DIAGNOSE AND TO TREAT
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DOI: 10.1136/annrheumdis-2019-eular.7398
Abstract: Background Fibrodysplasia ossificans progressiva (FOP) caused by mutations in the ACVR1 gene, which codes for activin receptor IA, a type I receptor of the bone morphogenetic protein (BMP) pathway. FOP is a very rare disease… read more here.
Keywords: diagnosis; fibrodysplasia ossificans; bilateral hallux; therapy ... See more keywords