Pediatric Scleroderma

Pediatric scleroderma is a rare autoimmune condition that occurs in children, where the body’s immune system mistakenly attacks its own tissues. This leads to the hardening and tightening of skin and connective tissues, affecting blood vessels and internal organs. Symptoms can include swelling, skin changes, and joint pain. The exact cause is unknown, but it may involve genetic and environmental factors. Treatment focuses on managing symptoms, improving quality of life, and preventing complications, often involving medications and physical therapy. Early diagnosis and a tailored care plan are essential for the best outcomes.