Results 31 to 40 of about 56,026 (190)

Fibrodysplasia ossificans progressiva: case report [PDF]

Arquivos 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, LUCIANO DE SOUZA QUEIROZ, ALLAN DE OLIVEIRA SANTOS, EDWALDO E CAMARGO, M VALERIANA L MOURA-RIBEIRO   +4 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, Vijaykrishna Chilakamarri, Prajnya Ranganath, Abhishek Jagdishchander Arora, Maria Celestina Vanaja   +4 more
doaj   +1 more source

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, Sascha Rausch, Uzma Arif, Bilal El Yafawi   +3 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., Tomić Jelena M., Vijatov-Đurić Gordana V., Radojčić Branka S., Vučković Nada M., Ćulafić Jelena N.   +5 more
doaj   +1 more source

Troubles oro-faciaux dans Fibrodysplasia ossificans progressiva. Revue systématique. [PDF]

, 2019
Fibrodysplasia ossificans progressiva (FOP) or myositis ossificans is a very rare autosomic dominant disease. Progressive ectopic bone formation occurs in ligaments, muscles and fascia and provoque severe movement limitation with time.
Garcia-Lopez, Carlos, Garcia, Paola, Coibion, France   +2 more
core   +3 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, T Evangelista, L Barroso, J Reis, A R Gomes   +4 more
doaj   +1 more source

Heterotopic ossification in a 7‐year‐old female patient treated with individualized homeopathy: A case report

Clinical Case Reports, Volume 7, Issue 12, Page 2526-2533, December 2019., 2019
Classical homeopathy can be included among the treatment options for congenital heterotopic ossification. Abstract Classical homeopathy can be included among the treatment options for congenital heterotopic ossification.
Dionysios Tsintzas, Atul Jaggi, Latika Jaggi, Seema Mahesh, George Vithoulkas   +4 more
wiley   +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, Akhil A Tawari, Arvind B Goregaonkar   +2 more
doaj   +1 more source

Fibrodysplasia ossificans progressiva: A case report

Asian Journal of Medical Sciences, 2014
Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder with unknown cause. Disease is characterized by heterotopic ossifications of connective tissue and congenital malformations of distal part of extremities.
Sreedhar Vasala
doaj   +1 more source

Heterotopic Ossification: A Comprehensive Review

JBMR 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, Jeffrey Lisiecki, Sarah Miller, Adam Levin, Laura Fayad, Catherine Ding, Takashi Sono, Edward McCarthy, Benjamin Levi, Aaron W James   +9 more
wiley   +1 more source