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Piebaldism is an uncommon autosomal dominant disorder characterized by the congenital absence of melanocytes in localised areas of the skin and hair due to c-kit gene mutation, which affects the differentiation and migration of melanoblasts from the neural crest during the embryonic life. This condition is clinically characterised by the presence of localized stable hypo to depigmentation of the skin and hair, and by a characteristic distribution that involves the anterior trunk, extremities, the central portion of eyebrows, and the midfrontal portion of scalp with resultant white forelock, which is also the most common and persisting feature [1].

Looking through the dermoscope in a case of piebaldism