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18 gru 2023 · Table of Contents. Localized Scleroderma. Systemic Sclerosis. Other Symptoms. Scleroderma is an autoimmune condition in which the body produces too much collagen. This affects the skin by causing it to be tight and shiny and can also affect internal organs, causing significant organ dysfunction.
• It’s estimated that there are 300,000 cases of scleroderma in the United States. • Women make up 80 percent of scleroderma cases, but men, young children and teens also get scleroderma. • Scleroderma typically strikes between the ages of 25 and 55. • In 95 percent of cases, scleroderma begins with Raynaud Phenomenon (hands and
8 lut 2023 · Scleroderma commonly affects people 30 to 50 years of age but is found in all ages. Also, women are typically more likely than men to receive a diagnosis of this condition.
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.
15 cze 2024 · Anyone can get scleroderma, but it is more common in people assigned female at birth. People typically get scleroderma between ages 30 and 50. Black people often have earlier onset and are more likely to have more skin involvement and lung disease.
The term scleroderma refers to hardened skin. There are various conditions that are affected by scleroderma or appear similar to it. Acrodermatitis chronica atrophicans. Systemic sclerosis and CRST syndrome. Mixed connective tissue disease. Porphyria cutanea tarda. Morphoea or localised scleroderma. Lipodermatosclerosis.
The following explains who has a higher risk of developing scleroderma. Gender: Women are more likely than men to get most types of scleroderma. One type, linear morphea, occurs about equally in men and women. Age: This disease can occur at any age. Children and seniors get scleroderma. One type, linear morphea, tends to develop before 18 years ...
