Scleroderma, or systemic sclerosis, is a rare but complex autoimmune disease that causes the skin to become unusually hard and tight. It occurs when the body’s immune system triggers an overproduction of collagen, the protein responsible for skin and connective tissue strength. This excess collagen builds up in the skin and, in more severe cases, in internal organs such as the lungs, heart, kidneys, and digestive tract. Scleroderma is typically categorized into two main types: limited and diffuse. The limited type generally affects smaller areas of skin, while the diffuse type involves larger portions and is more likely to include internal organs. There's also localized scleroderma (morphea), which affects only the skin and doesn’t involve internal systems. While the disease has no known cure, treatment is focused on managing symptoms, slowing progression, and preventing complications. A multidisciplinary approach involving rheumatologists, dermatologists, and pulmonologists is often needed. Early diagnosis and specialist care can make a significant difference in quality of life, mobility, and long-term outcomes. Get expert care from a trusted Scleroderma Treatment Specialist in DLF Phase 1, Dr. Naval Mendiratta.
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