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
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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
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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
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Bilateral myositis ossificans of the masseter muscle after chemoradiotherapy and critical illness neuropathy- report of a rare entity and review of literature [PDF]
, 2009 Myositis ossificans in the head and neck is a rare heterotropic bone formation within a muscle.
Astrid L Kruse +21 more
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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
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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
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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
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A case of Myositis ossificans traumatica on one skeleton from Viminacium [PDF]
, 2019 Rimski grad i vojni logor Viminacijum nalazi se između sela Stari Kostolac i Drmno, na 12 km severoistočno od Požarevca, u blizini ušća Mlave u Dunav (karta 1). Tokom svoje istorije postao je najveće urbano naselje i glavni grad provincije Gornje Mezije (
Mikić, Ilija +2 more
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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
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Fibrodyslasia (Myositis) ossificans progressiva- A case report [PDF]
, 2016 We are presenting a case report of an 18yr old kenyan girl with big toe/ thumb anomalies and a 3 year history of heterotopic ossification of the temporo-mandibular joints, cervical spine, shoulders, elbows, lumbar spine and abdominal wall.
Mead, TC, Muteti, EN
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