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Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome

10 Jan 2020

Abstract excerpt

Segmental progeroid syndromes are commonly represented by genetic conditions which recapitulate aspects of physiological aging by similar, disparate, or unknown mechanisms. Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease caused by mutations in the gene for ACVR1/ALK2 encoding Activin A receptor type I/Activin-like kinase 2, a bone morphogenetic protein (BMP) type I receptor, and results in...

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PMID: 31998237
DOI: 10.3389/fendo.2019.00908

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