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Fibrodysplasia ossificans progressiva [PDF]

Clinical Case Reports, 2023
Key Clinical Message Fibrodysplasia ossificans progressiva is a progressively debilitating condition associated with significant morbidity caused by heterotopic ossification. Recognition of the early signs of hallux valgus and painful soft tissue nodules
Chané Smit, André Uys
doaj   +5 more sources

Anesthetic and airway management for inguinal hernia repair in a pediatric patient with fibrodysplasia ossificans progressiva: a case report [PDF]

Journal of Medical Case Reports
Background Fibrodysplasia ossificans progressiva is a rare genetic disorder characterized by the progressive heterotopic ossification of soft connective tissues, ultimately leading to cumulative disability and ankylosis.
Saori Ozaki, Satoshi Kamiya, Noriko Takeno, Tomomi Ishii, Yukari Toyota, Hiroshi Yokomi, Takahiro Kato, Yasuo M. Tsutsumi   +7 more
doaj   +2 more sources

Fibrodysplasia ossificans progressiva associated with osteochondromatosis: A case report [PDF]

Radiology Case Reports
Fibrodysplasia ossificans progressiva is a rare and severely debilitating genetic disorder affecting approximately 1 in 2 million people. It is characterized by progressive heterotopic ossification of soft tissues, leading to the formation of ectopic ...
Jihane El Houssni, Sanae Jellal, Fariss Dehayni, Ismail Neftah, Siham El Haddad, Nazik Allali, Latifa Chat   +6 more
doaj   +2 more sources

Challenges in the diagnosis of fibrodysplasia ossificans progressiva with the ACVR1 mutation (c.774G > C, p.R258S): a case report and review of literature [PDF]

Orphanet Journal of Rare Diseases
The diagnosis of fibrodysplasia ossificans progressiva is missed or delayed because of its insidious precursors, especially in uncharacteristic cases.
Siqi Yang, Rongrong Cui, Jialin Li, Ruchun Dai   +3 more
doaj   +2 more sources

Immunologic Aspects in Fibrodysplasia Ossificans Progressiva [PDF]

Biomolecules
Background: Inflammation is a major driver of heterotopic ossification (HO), a condition of abnormal bone growth in a site that is not normally mineralized.
Anastasia Diolintzi, Mst Shaela Pervin, Edward C. Hsiao   +2 more
doaj   +2 more sources

Cardiopulmonary and Neurologic Dysfunctions in Fibrodysplasia Ossificans Progressiva

Biomedicines, 2021
Fibrodysplasia Ossificans Progressiva (FOP) is an ultra-rare but debilitating disorder characterized by spontaneous, progressive, and irreversible heterotopic ossifications (HO) at extraskeletal sites.
Xiaobing Yu, Edward Hsiao, Yu Xiaobing   +2 more
exaly   +3 more sources

Fibrodysplasia ossificans progressiva: Two case reports [PDF]

Radiology Case Reports
Fibrodysplasia ossificans progressiva (FOP) is a rare and progressively debilitating disorder affecting 1 in 2 million individuals. It is characterized by the progressive ossification of soft tissues into ectopic bone and congenital malformations of the ...
Yodit Abraham Yaynishet, Fathia Omer Salah, Bemnet Taye Gebregiorgis, Abdulmejid Suleyman Mume, Henok Dessalegn Damtew, Tinsae Zelalem Amare, Tilahun Mengistu Manaleh   +6 more
doaj   +2 more sources

Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome

Frontiers in Endocrinology, 2020
Segmental progeroid syndromes are commonly represented by genetic conditions which recapitulate aspects of physiological aging by similar, disparate, or unknown mechanisms.
Robert Pignolo, Frederick Kaplan, Pignolo Robert J   +2 more
exaly   +3 more sources

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

National Journal of Medical Research, 2013
Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities.
Mehul M Gosai, Hareshwaree B Hariyani, Monil Shah, Payal H Purohit, Mihir A Sadadia   +4 more
doaj   +1 more source

Fibrodysplasia Ossificans Progressiva

Neurology India
Abstract: Fibrodysplasia Ossificans Progressiva (FOP), commonly known as Stoneman Syndrome, is an ultra-rare genetic disorder characterized by the progressive ossification of soft tissues, leading to the formation of a secondary skeleton. This paper provides a comprehensive analysis of FOP, examining its epidemiology, pathophysiology, clinical ...
Agrawal U, Tiwari V.
europepmc   +5 more sources