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5 kwi 2024 · Systemic sclerosis exhibits a female predominance with a female-to-male ratio of about 5:1. Females typically develop the condition at an earlier age than males. The peak age of onset is between 45 and 54 in African-American females and between 55 and 64 in European-American females.
Scleroderma typically strikes between the ages of 25 and 55. In 95 percent of cases, scleroderma begins with Raynaud Phenomenon (hands and feet abnormally sensitive to cold). Federal funding for scleroderma research lags behind funding for other diseases of similar prevalence.
Although patients who develop scleroderma (SSc) later in life (≥ 65 years) may express the entire clinical spectrum of disease, we hypothesize that patients with late-age onset incur a different risk for specific organ manifestations of disease compared to those with younger-age onset SSc.
The most common age to develop scleroderma is between 35 and 50 years of age. Young children and older adults can also develop scleroderma. What are the early signs of Scleroderma?
6 cze 2020 · AGING IN SCLERODERMA. With an average age of diagnosis between 45 and 64 years, SSc is not traditionally regarded as a disease of aging.
3 lut 2022 · Scleroderma renal crisis is usually diagnosed within 5 years of SSc onset with features that include hypertension, edema, and electrolyte abnormalities. Most SSc patients experience GI (eg, gastroesophageal reflux disease, GI dysmotility) and urologic manifestations (sexual dysfunction).
Both forms of the disease can affect people of any age, but systemic scleroderma is most commonly diagnosed in people between ages 20 and 50 and rarely occurs in children. There is no cure for scleroderma. In many cases, damage caused by the condition cannot be reversed.
