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Disease aggravation following surgery in a rare patient suspected to Fibrodysplasia (Myositis) ossificans progressiva: a case report [PDF]
Background Fibrodysplasia ossificans progressiva (FOP) as a rare and heritable disorder with the infrequent genetic transmission of the condition is a catastrophic disorder of heterotopic ossification (HO) and a cause of extraskeletal bone formation in ...
Amir Zarei +4 more
doaj +2 more sources
Temporomandibular joint ankyloses (TMJA) may manifest in patients with several predisposing systemic conditions. A case of extraarticular TMJA is presented in a patient diagnosed with fibrodysplasia ossificans progressive (FOP) is presented. The features,
Kavish Kapoor +3 more
doaj +2 more sources
Fibrodysplasia Ossificans Progressiva: Clinical and Genetic Aspects [PDF]
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in ...
Pignolo Robert J +2 more
doaj +4 more sources
Research trends and hotspots of myositis ossificans: a bibliometric analysis from 1993 to 2022 [PDF]
Myositis ossificans (MO) is characterized by benign heterotopic ossificans in soft tissues like muscles, which can be classified into nonhereditary MO and fibrodysplasia ossificans progressiva (FOP). Although MO has been studied for decades, no research
Bowen Lai +3 more
doaj +2 more sources
Fibrodysplasia ossificans progressiva: case report [PDF]
Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities.
ANAMARLI NUCCI +4 more
doaj +4 more sources
Fibrodysplasia Ossificans Progressive: A Case Report on Rare Musculoskeletal Disorder [PDF]
Fibrodysplasia Ossificans Progressive (FOP) (also known as Myositis ossificans progressiva/Stone man disease/Munchmeyer’s disease) is one of the unfamiliar congenital disorders affecting the musculoskeletal system.
Manoj Arya +4 more
doaj +1 more source
Pediatric myositis ossificans circumscripta following traumatic hip dislocation: A case report
Myositis ossificans is non-neoplastic heterotopic bone forms in skeletal muscle. We recognize 3 subtypes: fibrodysplasia ossificans progressiva, myositis ossificans with no history of trauma (nontraumatic or pseudomalignant), and circumscribed or ...
Khadija Laasri, MD +5 more
doaj +1 more source
Knowledge and awareness about fibrodysplasia ossificans progressiva among dental students
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder which is autosomal dominant distinguished by congenital malformations of large toes and flare ups, etc. It is a disorder of connective tissue, with heterotopic ossifications seen with
L Akshayaa +3 more
doaj +1 more source
Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare genetic disorder characterized by the progressive formation of heterotopic bone in soft tissues.
Mohammed Mostafa Kotb +2 more
doaj +1 more source
Fibrodysplasia Ossificans Progressiva: A Case Report
Fibrodysplasia ossificans progressiva is a genetic disorder of the connective tissue differentiation characterized by congenital malformation of the big toes and progressive heterotopic ossification in the extra skeletal tissues like tendons, ligaments,
Sudeep Acharya +2 more
doaj +1 more source

