Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Myositis ossificans progressiva"'
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-4 (2023)
Abstract 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 f
Externí odkaz:
https://doaj.org/article/b888558a36944555b20e9bffe77df63d
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract 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.
Externí odkaz:
https://doaj.org/article/263834835d0741e4b44b01084f13d8ea
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract 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 b
Externí odkaz:
https://doaj.org/article/d3b01752b3aa4f9dbe1454369b858da4
Akademický článek
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Publikováno v:
Oman Medical Journal, Vol 29, Iss 5, Pp 368-370 (2014)
Fibrodysplasia ossificans progressiva formerly known as Myositis ossificans progressiva is a rare hereditary mesodermal disorder. It is characterized by congenital skeletal anomalies and progressive ectopic bone formation in connective tissue, result
Externí odkaz:
https://doaj.org/article/9ae9b5e21cb04f488e49c2acec6c1efa
Autor:
Sreedhar Vasala
Publikováno v:
Asian Journal of Medical Sciences, Vol 5, Iss 4, Pp 113-115 (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. Most cases are sporadic and t
Externí odkaz:
https://doaj.org/article/b7223401f7204902a9782116d3ff44c4
Publikováno v:
Annals of Indian Academy of Neurology, Vol 11, Iss 2, Pp 119-122 (2008)
An 8-year-old boy, diagnosed as cervical dystonia, was referred to our tertiary center. After a trivial trauma he had developed painful lumps in the axial region, which was followed by restricted movements of neck, shoulder, and abdominal muscles ove
Externí odkaz:
https://doaj.org/article/1db313bc72a34ed3bf56e50f89aba4cb
Autor:
Maheshwar Lakkireddy, Vijaykrishna Chilakamarri, Prajnya Ranganath, Abhishek Jagdishchander Arora, Maria Celestina Vanaja
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 8, Pp RD01-RD03 (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 po
Externí odkaz:
https://doaj.org/article/c750a9527258453ba267515ad1fd45aa
Autor:
Andre Leite Gonçalves, Marcelo Rodrigues Masruha, Carmelinda Correia de Campos, Patricia Longo Ribeiro Delai, Luiz Celso Pereira Vilanova
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 4, Pp 1090-1093 (2005)
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder characterized by postnatal progressive heterotopic ossification of the connective tissue and congenital malformation of the big toes. We report on a nine-year-old girl
Externí odkaz:
https://doaj.org/article/5c2143bab6ee45ffb71e33fd87462fea
Publikováno v:
Indian Journal of Nuclear Medicine : IJNM : The Official Journal of the Society of Nuclear Medicine, India
Fibrodysplasia ossificans progressiva is a rare genetic disease believed to occur in approximately 1 in 2 million people worldwide and is characterized by progressive extraosseous ossification over the course of a lifetime in an inevitable and unpred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70b324f2b606187c1e1b61aa89b962f
http://europepmc.org/articles/PMC6593934
http://europepmc.org/articles/PMC6593934