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Bishoy Raafat Zaky

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Open access Aug 2026

Tracking the Course of Fibrodysplasia Ossificans Progressiva in a Patient with the Classic ACVR1 Mutation

Fibrodysplasia Ossificans Progressiva (FOP) is an extremely rare and debilitating genetic disease affecting approximately 1 in 2 million people. It is caused by a heterozygous gain-of-function mutation in the gene encoding activin A receptor type I (ACVR1), leading to dysregulated bone morphogenetic protein (BMP) signa...

M. Kotb, Usama Farghaly Omar, Bishoy Raafat Zaky et al. · 0 citations

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