Results 1 to 10 of about 56,026 (190)

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

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   +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

Myositis Ossificans Progressiva: Case Report [PDF]

open access: yesRevista Brasileira De Ortopedia, 2012
Frederico Barra de Moraes
exaly   +2 more sources

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

Knowledge and awareness about fibrodysplasia ossificans progressiva among dental students

open access: yesJournal of Advanced Pharmaceutical Technology & Research, 2022
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: A Case Report

open access: yesJournal of Nepal Health Research Council, 2018
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

Living with Fibrodysplasia Ossificans Progressiva: Radiological Images of a Patient with Extensive Heterotopic Ossification

open access: yesDiagnostics, 2023
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: Literature Review and Case Report

open access: yesВопросы современной педиатрии, 2023
Background. Fibrodysplasia ossificans progressiva (FOP) is a genetic disease of the heterotopic ossification group associated with the mutation in ACVR1/ALK2 gene.
Natalya N. Korableva   +3 more
doaj   +1 more source

Miosite ossificante progressiva: uma perspectiva no controle da doença A perspective on the control of myositis ossificans progressiva

open access: yesJornal de Pediatria, 2001
OBJETIVO: relatar quatro casos de miosite ossificante progressiva, forma de apresentação da doença e novas medidas de controle e tratamento. DESCRIÇÃO: os autores descrevem quatro casos de miosite ossificante progressiva.
Durval B. Palhares, Lígia M. Leme
doaj   +1 more source

Home - About - Disclaimer - Privacy