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Scleroderma
Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc).
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Systemic sclerosis 261 trials · 295 incl. sub-types Sub-types →
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Localized scleroderma 14 trials · 15 incl. sub-types Sub-types →
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Neonatal scleroderma 0 trials