Results 31 to 40 of about 1,795 (202)
The Turkish Journal of Pediatrics, 2018 Fibrodysplasia ossificans progressiva is one of the most devastating disorder of mankind characterized by progressive heterotopic ossification. Apart from hallux valgus, other symptoms start to develop in the first decade of life.
Mustafa Çakan +3 more
doaj +1 more source
Nodular osteochondrogenic activity in soft tissue surrounding osteoma in neurogenic para osteo-arthropathy: morphological and immunohistochemical study [PDF]
, 2004 Background Neurogenic Para-Osteo-Arthropathy (NPOA) occurs as a consequence of central nervous system injuries or some systemic conditions. They are characterized by bone formation around the main joints.
T Youssefian +50 more
core +2 more sources
Fibrodysplasia ossificans progressiva (stone man syndrome): a case report
Journal of Medical Case Reports, 2019 Background Fibrodysplasia ossificans progressiva is an ultrarare autosomal dominant disorder and disabling syndrome characterized by postnatal progressive heterotopic ossification of the connective tissue and congenital malformation of the big toes ...
Zakir Ali Shah +3 more
doaj +1 more source
Clinical and Genetic Analysis of Fibrodysplasia Ossificans Progressiva: A Case Report and Literature Review [PDF]
Journal of Clinical and Diagnostic Research, 2015 Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by congenital malformation of the great toes and disabling heterotopic ossification in specific anatomic locations with a world wide prevalence of 1 in 2 million ...
Maheshwar Lakkireddy +4 more
doaj +1 more source
Dystrophic calcifications and Raynaud’s phenomenon in an eight-year old girl [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2014 Introduction. Dystrophic calcifications are the most common subtype of skin calcinosis. Tumorous soft tissue calcium deposits usually contain hydroxyapatite and amorphous calcium phosphate.
Grebeldinger Slobodan P. +5 more
doaj +1 more source
Fibroplasia Ossificans Progressiva: A Case Report of a Rare Disease Entity [PDF]
, 2019 BACKGROUND: Fibrodysplasia ossificans progressiva (FOP), also known as Myositis ossificans progressiva or Munchmeyer's disease, is an extremely rare and disabling genetic condition of congenital skeletal malformations and progressive heterotopic ...
Gorfy, Yocabel +3 more
core +2 more sources
Fibrodysplasia Ossificans Progressiva: Case Report. [PDF]
, 2015 Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities.
Camargo, E E +4 more
core +1 more source
Miosite ossificante progressiva. Stone man.
Acta Médica Portuguesa, 2001 Myositis ossificans progressiva (MOP) is a rare hereditary connective tissue disease, genetically inherited as an autossomal dominant trait with complete penetrance but variable expression.
J E Fonseca +4 more
doaj +1 more source
Fibrodysplasia Ossificans Progressiva: A Case Report
Journal of Orthopaedic Surgery, 2013 Fibrodysplasia ossificans progressiva or myositis ossificans is a rare disease characterised by bony deposits or the ossification of soft tissues. It transforms skeletal muscles, tendons, ligaments, fascia, and aponeuroses into heterotopic bony deposits ...
Anoop C Dhamangaonkar +2 more
doaj +1 more source
Myositis ossificans in a child athlete: a case study [PDF]
, 2022 Background: A 13-year-old female athlete presented with a painful lesion in her right buttock for which she had been receiving physiotherapy. It was keeping her from participating in sports.
Gounder, Perusha +10 more
core +2 more sources