Palovarotene for Fibrodysplasia Ossificans Progressiva (FOP): Results of a Randomized, Placebo‐Controlled, Double‐Blind Phase 2 Trial
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Bone and Mineral Research"
DOI: 10.1002/jbmr.4655
Abstract: Fibrodysplasia ossificans progressiva (FOP) is an ultra‐rare genetic disorder characterized by progressive heterotopic ossification (HO), often heralded by flare‐ups, leading to reduced movement and life expectancy. This placebo‐controlled, double‐blind trial (NCT02190747) evaluated palovarotene, an orally… read more here.
Keywords: progressiva fop; placebo; ossificans progressiva; week ... See more keywords
Evolution of heterotopic bone in fibrodysplasia ossificans progressiva: An [18F]NaF PET/CT study.
Sign Up to like & getrecommendations! Published in 2019 at "Bone"
DOI: 10.1016/j.bone.2019.03.009
Abstract: Fibrodysplasia ossificans progressiva (FOP) is a rare, autosomal dominant disorder characterized by heterotopic ossification (HO) in muscles, ligaments and tendons. Flare-ups often precede the formation of HO, resulting in immobilization of joints. Due to progression… read more here.
Keywords: 18f naf; ossificans progressiva; naf pet; fibrodysplasia ossificans ... See more keywords
Self-reported baseline phenotypes from the International Fibrodysplasia Ossificans Progressiva (FOP) Association Global Registry.
Sign Up to like & getrecommendations! Published in 2020 at "Bone"
DOI: 10.1016/j.bone.2020.115274
Abstract: A global, patient-reported registry has been established to characterize the course of disease and track clinical outcomes in patients with fibrodysplasia ossificans progressiva (FOP), an ultra-rare genetic condition of progressive heterotopic ossification (HO) that results… read more here.
Keywords: progressiva fop; fibrodysplasia ossificans; baseline phenotypes; fop association ... See more keywords
Late-onset fibrodysplasia ossificans progressiva with atypical presentation: A case report
Sign Up to like & getrecommendations! Published in 2019 at "Case Reports in Women's Health"
DOI: 10.1016/j.crwh.2019.e00134
Abstract: Fribrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by progressive heterotopic ossification of connective tissues, episodic flare-ups and bilateral deformities of the great toe (hallux valgus). As faulty tissue repair processes progressively calcify… read more here.
Keywords: hallux valgus; late onset; fibrodysplasia ossificans; case ... See more keywords
The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call.
Sign Up to like & getrecommendations! Published in 2017 at "European journal of medical genetics"
DOI: 10.1016/j.ejmg.2017.04.013
Abstract: BACKGROUND Congenital bilateral hallux valgus with associated absence or fusion of the interphalangeal joint is a classic diagnostic feature of fibrodysplasia ossificans progressiva (FOP), a human genetic disease of extra-skeletal bone formation caused in nearly… read more here.
Keywords: great toe; fibrodysplasia ossificans; toe malformation; malformation ... See more keywords
Insights into the biology of fibrodysplasia ossificans progressiva using patient-derived induced pluripotent stem cells☆
Sign Up to like & getrecommendations! Published in 2019 at "Regenerative Therapy"
DOI: 10.1016/j.reth.2019.04.004
Abstract: The demand for development of new drugs remains on the upward trend because of the large number of patients suffering from intractable diseases for which effective treatment has not been established yet. Recently, several researchers… read more here.
Keywords: fibrodysplasia ossificans; ossificans progressiva; biology; pluripotent stem ... See more keywords
Generation of Fibrodysplasia ossificans progressiva and control integration free iPSC lines from periodontal ligament fibroblasts.
Sign Up to like & getrecommendations! Published in 2019 at "Stem cell research"
DOI: 10.1016/j.scr.2019.101639
Abstract: Fibrodysplasia ossificans progressiva (FOP) is a very rare devastating heterotopic ossification disorder, classically caused by a heterozygous single point mutation (c.617G>A) in the ACVR1gene, encoding the Bone morphogenetic protein (BMP) type I receptor, also termed… read more here.
Keywords: periodontal ligament; fibrodysplasia ossificans; control; generation ... See more keywords
Gene Therapy for Fibrodysplasia Ossificans Progressiva: Feasibility and Obstacles
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DOI: 10.1089/hum.2022.023
Abstract: Fibrodysplasia ossificans progressiva (FOP) is a rare and devastating genetic disease, in which soft connective tissue is converted into heterotopic bone through an endochondral ossification process. Patients succumb early as they gradually become trapped in… read more here.
Keywords: fibrodysplasia ossificans; gene; ossificans progressiva; gene therapy ... See more keywords
AB1029 FIBRODYSPLASIA OSSIFICANS PROGRESSIVA: A CHALLENGE TO DIAGNOSE AND TO TREAT
Sign Up to like & getrecommendations! Published in 2019 at "Annals of the Rheumatic Diseases"
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
Surgical management of bilateral hip fractures in a patient with fibrodysplasia ossificans progressiva treated with the RAR-γ agonist palovarotene: a case report
Sign Up to like & getrecommendations! Published in 2020 at "BMC Musculoskeletal Disorders"
DOI: 10.1186/s12891-020-03240-2
Abstract: Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare disorder marked by painful, recurrent flare-ups and heterotopic ossification (HO) in soft and connective tissues, which can be idiopathic or provoked by trauma, illness, inflammation, or surgery.… read more here.
Keywords: surgery; fibrodysplasia ossificans; palovarotene; fracture ... See more keywords
Current challenges and opportunities in the care of patients with fibrodysplasia ossificans progressiva (FOP): an international, multi-stakeholder perspective
Sign Up to like & getrecommendations! Published in 2022 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-022-02224-w
Abstract: Background Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare, disabling genetic disorder characterized by congenital malformations of the great toes and progressive heterotopic ossification of soft and connective tissues. Assiduous attention to the unmet needs of… read more here.
Keywords: care; individuals fop; access; fibrodysplasia ossificans ... See more keywords