Abstract
Scleroderma is a rare disease. About 1-3% of all Scleroderma patients have disease onset before 16 years of age. It is categorized in two different subtypes, Systemic and Localized, being the last predominant in the pediatric age range. Localized Scleroderma encompasses different skin lesions like Morphea, Linear Scleroderma, En coup de sabre and Facial hemiatrophy also called Parry-Rombe…