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
Rare diseases: matching wheelchair users with rare metabolic, neuromuscular or neurological disorders to electric powered indoor/outdoor wheelchairs (EPIOCs) [PDF]
, 2015 Purpose: To describe the clinical features of electric powered indoor/outdoor wheelchair (EPIOC) users with rare diseases (RD) impacting on EPIOC provision and seating. Method: Retrospective review by a consultant in rehabilitation medicine of electronic
Andrew O. Frank +18 more
core +3 more sources
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
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
From variome to phenome : pathogenesis, diagnosis and management of ectopic mineralization disorders [PDF]
, 2015 Ectopic mineralization - inappropriate biomineralization in soft tissues - is a frequent finding in physiological aging processes and several common disorders, which can be associated with significant morbidity and mortality.
De Vilder, eva, Vanakker, Olivier
core +2 more sources
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
core +2 more sources