Results 1 to 10 of about 1,762 (159)

Disease aggravation following surgery in a rare patient suspected to Fibrodysplasia (Myositis) ossificans progressiva: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2023
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 ankylosis—“Knowing when not to operate”: Case report and qualitative systematic review of literature

open access: yesClinical Case Reports, 2022
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]

open access: yesOrphanet Journal of Rare Diseases, 2011
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   +3 more sources

Heterotopic Ossification: A Comprehensive Review [PDF]

open access: yesJBMR Plus, Volume 3, Issue 4, April 2019., 2019
ABSTRACT Heterotopic ossification (HO) is a diverse pathologic process, defined as the formation of extraskeletal bone in muscle and soft tissues. HO can be conceptualized as a tissue repair process gone awry and is a common complication of trauma and surgery.
Carolyn Meyers   +9 more
wiley   +2 more sources

Diagnosis of Pediatric Myositis Ossificans Based on Cytomorphology and Molecular Analysis From FNAB Sample: A Case Report. [PDF]

open access: yesDiagn Cytopathol
ABSTRACT Myositis ossificans (MO) is a benign soft tissue lesion, characterized by ectopic ossification due to inappropriate fibroblast differentiation, most commonly affecting skeletal muscles. It often occurs in young adults after muscle trauma, predominantly in male patients and very rarely in children. We describe the case of a previously healthy 3‐
Ledinek Ž   +7 more
europepmc   +2 more sources

Early Detection for Better Patient Outcome: A Case Report on Two Patients Presenting With Fibrodysplasia Ossificans Progressiva at Tikur Anbessa Specialized Hospital, Ethiopia. [PDF]

open access: yesCase Rep Orthop
Fibrodysplasia ossificans progressiva is an ultrarare disorder of endochondral ossification. It is unfamiliar to most care providers in low‐income countries such as Ethiopia. Even though the clinical presentation is typical, most cases remain misdiagnosed in our region.
Haile AM, Azale AW, Ayana B.
europepmc   +2 more sources

Research trends and hotspots of myositis ossificans: a bibliometric analysis from 1993 to 2022 [PDF]

open access: yesEFORT Open Reviews
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]

open access: yesArquivos de Neuro-Psiquiatria, 2000
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

Pediatric myositis ossificans circumscripta following traumatic hip dislocation: A case report

open access: yesRadiology Case Reports, 2023
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

Fibrodysplasia Ossificans Progressive: A Case Report on Rare Musculoskeletal Disorder [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
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

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