Results 21 to 30 of about 1,793 (201)
Myositis Ossificans Presenting as a Rapidly Enlarging Neck Mass With Dyspnea
, 2022 OTO Open, Volume 6, Issue 3, July‐September 2022.
Haley Hullfish +3 more
wiley +1 more source
Miosite ossificante progressiva: relato de caso Myositis ossificans progressiva: case report
Revista Brasileira de Ortopedia, 2012 A miosite ossificante progressiva é uma doença rara, com menos de 1.000 casos descritos, autossômica dominante. O paciente apresenta edemas, devidos a processos inflamatórios, que vão se calcificando, com perda da mobilidade da região afetada. O objetivo
Frederico Barra de Moraes +6 more
doaj +1 more source
Chronic intoxication by ethane-1-hydroxy-1,1-diphosphonate (EHDP) in a child with myositis ossificans progressiva. [PDF]
, 1993 Chronic intoxication by ethane-1-hydroxy-1,1-diphosphonate (EHDP) in a child with myositis ossificans progressiva.
Beluffi G +4 more
core +1 more source
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
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
Myositis ossificans in the newborn. A case report. [PDF]
, 1986 Myositis ossificans (MO) and fibroosseous pseudotumor of digits (FP) are pseudotumoral mimics of malignancy. A review of 50 cases of MO and 14 cases of FP showed that a malignant diagnosis was suggested by referring pathologists in 23% of MO and 9% of FP.
Beluffi G +5 more
core +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
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
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
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