Results 21 to 30 of about 1,444 (153)
Fibrodysplasia Ossificans Progressiva - Radiological Findings: A Case Report
Oman Medical Journal, 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, resulting ...
Ishaq Al-Salmi +2 more
doaj +1 more source
Learning Health Systems, Volume 4, Issue 4, October 2020., 2020 Abstract Background This study is part of the EU‐funded project HarmonicSS, aimed at improving the treatment and diagnosis of primary Sjögren's syndrome (pSS). pSS is an underdiagnosed, long‐term autoimmune disease that affects particularly salivary and lachrymal glands.
Sytske Wiegersma +6 more
wiley +1 more source
Myositis ossificans traumatica of the masticatory muscles: etiology, diagnosis and treatment
Head & Face Medicine, 2018 Background Myositis ossificans describes a heterotopic bone formation within a muscle. Thereby myositis ossificans is classified in two different groups: myositis ossificans progressiva (MOP) which describes a genetic autosomal dominant rare disease and ...
Marcel Hanisch +5 more
doaj +1 more source
International Journal of Osteoarchaeology, Volume 30, Issue 3, Page 410-414, May/June 2020., 2020 Abstract This case study documents an unusual heterotopic ossification with associated pseudarthroses of the lumbar spine. We examined the partial skeletal remains of an adult from a Late Bronze Age (Mycenaean Late Helladic IIB‐IIIA1 period, approximately1400–1375 BCE) chamber tomb from the Athenian Agora excavations in Greece.
Susan Kirkpatrick Smith, Maria A. Liston
wiley +1 more source
Myositis ossificans progressiva
RoFo Fortschritte Auf Dem Gebiet Der Rontgenstrahlen Und Der Bildgebenden Verfahren, 1992 R P, Agarwal +4 more
exaly +2 more sources
Arquivos de Neuro-Psiquiatria, 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 with
Andre Leite Gonçalves +4 more
doaj +1 more source
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 +4 more
doaj +1 more source
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
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
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