Scleroderma is likely caused by a combination of factors, including an external trigger (infection or other exposure) and a genetic predisposition. The Scleroderma Registry will conduct genetic analyses for disease-related genes in patients with scleroderma and their family members (parents, brothers, and sisters).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Establish National registry of Scleroderma as resource for scleroderma scientific community
Timeframe: ongoing