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Spondylosis is caused from years of constant abnormal pressure, caused by joint subluxation, stress induced by sports, acute and/or repetitive trauma, or poor posture, being placed on the vertebrae and the discs between them. The abnormal stress causes the body to form new bone in order to compensate for the new weight distribution.
Spondylolysis is a defect or stress fracture in the pars interarticularis of the vertebral arch. [1] The vast majority of cases occur in the lower lumbar vertebrae (L5), but spondylolysis may also occur in the cervical vertebrae .
Spondylolisthesis is when one spinal vertebra slips out of place compared to another. [1] While some medical dictionaries define spondylolisthesis specifically as the forward or anterior displacement of a vertebra over the vertebra inferior to it (or the sacrum ), [ 2 ] [ 3 ] it is often defined in medical textbooks as displacement in any ...
Spondylolisthesis is the forward displacement of a vertebra and retrolisthesis is a posterior displacement of one vertebral body with respect to the adjacent vertebra to a degree less than a dislocation. Spondylolysis, also known as a pars defect, is a defect or fracture at the pars interarticularis of the vertebral arch.
Given the well-established familial aggregation and the concordance rate of up to 63% in identical twins (vs 23% in nonidentical twins), it is evident that genetic variables play a role in the susceptibility to ankylosing spondylitis. [14] [15] There is limited research on familial aggregation in other forms of spondyloarthritis. [12]
Spondylitis; Spondylitis due to Tropheryma whipplei: Contrast-enhanced, T1 weighted fat suppressed magnetic resonance imaging demonstrating contrast enhancing lesions of spondylitis in the first (L1) and second (L2), as well as fourth (L4) and fifth (L5) lumbar vertebra, sparing the intervertebral discs
SMA is a category of spinal disease that in linked with genetic disorders. More specifically, it is caused by an autosomal recessive disorder due to a homozygous mutation of a motor neuron gene. [3]
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