Search results
RESULTS. Overall, 2084 (91%) patients developed SSc prior to age 65; whereas 216 (9%) were ≥65 years. Late-age onset patients had a significantly higher proportion of anti-centromere antibodies (42% vs 27%; p=0.001) compared to younger-age onset.
1 sty 2011 · The age of scleroderma onset can impact the course of disease and increase the risk for organ-specific complications such as pulmonary vascular disease. As individuals age with scleroderma, physicians should focus on careful monitoring of each organ system and comprehensive medical care.
9 sty 2023 · The five-year survival rate (that is, patients who are still alive 5 years following diagnosis) among patients with diffuse cutaneous systemic sclerosis is about 84%. Five-year survival among patients with limited skin (cutaneous) systemic sclerosis is high — over 90%.
Here is what is included in this Guide: Scleroderma Overview –This initial section gives a general description of the scleroderma family of diseases and discusses the affected population, possible causes, and typical symptoms.
It is estimated that there are over 6000 people with systemic scleroderma in Australia. Statistically, approximately three to four times more women than men develop the condition. Scleroderma is found in every age group from infants to the elderly, but its onset is most frequent between the ages of 25 to 55.
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.
In late 2013, the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) approved a new set of diagnostic criteria for systemic sclerosis (SSc), replacing the older 1980 diagnostic criteria.
