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Review: Fibrodysplasia Ossificans Progressiva
Journal: International Research Journal of Pharmacy and Medical Sciences (IRJPMS) (Vol.7, No. 6)Publication Date: 2024-11-11
Authors : Vankodoth Sireesha Faiqua Fatima Shafeen Sultana Shiva Sai Kumar;
Page : 1-2
Keywords : ACVR1 Gene Mutation; Bone Morphogenetic Protein (BMP) Signaling; Endochondral Ossification; Fibrodysplasia Ossificans Progressiva; Future Therapies in FOP; Genetic Disorder; Heterotopic Ossification;
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Abstract
—Fibrodysplasia Ossificans Progressiva (FOP) is an ultra-rare genetic disorder characterized by heterotopic ossification of connective tissues and progressive loss of mobility. FOP is caused by mutations in the ACVR1 gene, leading to abnormal bone formation in muscles, tendons, and ligaments. This review explores the clinical features, genetic basis, pathophysiology, current management, and future directions for research and therapy
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Last modified: 2024-11-17 20:10:58