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We therefore cannot exclude that a few individuals exposed to both skin trauma and certain mineral-oil-containing cosmetics may develop arthritis, but this is unlikely to be a common event.
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Indeed, mice with defective NOX2 oxidase may even develop arthritis spontaneously (33).
Indeed, some patients with SLE may develop erosive arthritis (a rare syndrome often called "rhupus") in the context of circulating anti-CCP antibodies and alleles of MHC class II molecules including HLA-DRB1 and -DQB1 [ 31, 32].
Complicated cases may go on to develop arthritis, spondylitis, sacroiliitis, osteomyelitis, meningoencephalitis, and endocarditis.
The incidence of arthritis indicates the percentage of mice that develop arthritis.
Control BALB/c mice (n = 10) did not develop arthritis (arthritis score = 0) after zymosan administration.
These Tg mice did not spontaneously develop arthritis or cancer.
These mice develop arthritis spontaneously at 5 weeks of age.
Without this relieving mechanism, the ankle may develop secondary degenerative arthritis.
Major health consequences, such as neurological conditions and reactive arthritis, may develop in a small number of cases.
In rare cases, Beagles may develop immune mediated polygenic arthritis (where the immune system attacks the joints) even at a young age.
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