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Prognosis is typically worse for men and children than for women; however, if symptoms are present after age 60, the disease tends to run a more benign course. Early mortality, within five years, is due to organ failure or overwhelming infections, both of which can be altered by early diagnosis and treatment.
Although the age at which the disease manifests itself varies as well, most patients are between 30 and 60 years old. [3] The median age was 41 years old in a set of 40 cases, [6] and 42 years old in another Spanish series. [3] Asian patients appear to be affected by lupus erythematosus panniculitis at a slightly younger age group, with a mean ...
Lupus occurs from infancy to old age, with peak occurrence between ages 15 and 40. [20] Lupus affects females in the US 6 to 10 times more often than males. [20] Prevalence data are limited. Estimates vary and range from 1.8 to 7.6 cases per 100,000 persons per year in parts of the continental United States. [20]
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Childhood-onset systemic lupus erythematosus (i.e., cSLE), also termed juvenile-onset systemic lupus erythematosus, juvenile systemic lupus erythematosus, and pediatric systemic lupus erythematosus, is a form of the chronic inflammatory and autoimmune disease, systemic lupus erythematosus (i.e., SLE), that develops in individuals up to 18 years old. [1]
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In 1999 a study noted, "In recent years there has been growing concern regarding the diagnosis of incomplete forms of the autoimmune diseases" [26] and the first classification criteria were proposed in that year. [1] Historically the condition was sometimes called undifferentiated connective tissue syndrome, latent lupus or incomplete lupus. [1]
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