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Secondary synovial chondromatosis is the more common form and often occurs when there is pre-existent osteoarthritis, rheumatoid arthritis, osteonecrosis, osteochondritis dissecans, neuropathic osteoarthropathy (which often occurs in diabetic individuals), tuberculosis, or osteochondral fractures (torn cartilage covering the end of a bone in a ...
Synovial osteochondromatosis (SOC) (synonyms include synovial chondromatosis, primary synovial chondromatosis, synovial chondrometaplasia) is a rare disease that creates a benign change or proliferation in the synovium or joint-lining tissue, which changes to form bone-forming cartilage. In most occurrences, there is only one joint affected ...
Proton density-weighted image of a knee with synovial chondromatosis Proton density (PD)- weighted images are created by having a long repetition time (TR) and a short echo time (TE). [ 36 ] On images of the brain, this sequence has a more pronounced distinction between grey matter (bright) and white matter (darker grey), but with little ...
Ultrasound allows evaluation of joint effusion, synovial thickening and neovascularity, the bone/cartilage contour, and the femoral head-neck alignment. Although sonography is extremely sensitive in detecting increased synovial fluid, it is nonspecific and cannot be used with accuracy to determine the type of fluid.
"Synovial chondromatosis in the temporomandibular joint complicated by displacement and calcification of the articular disk: Report of two cases". American Journal of Neuroradiology. 22 (6): 1203–6. PMID 11415920. McCarty, William L; Farrar, William B (1979). "Surgery for internal derangements of the temporomandibular joint".
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Synovial osteochondromatosis; References. External links This page was last edited on 4 September 2021, at 16:03 (UTC). Text is available under the Creative ...
Familial synovial chondromatosis with dwarfism is a rare genetic disorder characterized by a combination of both synovial chondromatosis and dwarfism. [ 1 ] [ 2 ] Only 3 families from Germany and the United States worldwide have been described with the disorder, and they showed either X-linked or autosomal dominant inheritance.