eng Science and Education Publishing American Journal of Medical Case Reports 2374-216X 2025-09-10 13 8 50 51 10.12691/ajmcr-13-8-2 AJMCR20251382 article Professor Khitam Al-Refu Alrefukhi@yahoo.com 1 Heba Al-lala 2 Hiba Harbi 3 Faculty of Medicine, Muta University School of Medicine, the University of Jordan, Amman 11418, Jordan Karak Teaching Hospital. Muta University Piebaldism is a rare autosomal dominant genetic disorder characterized by congenitalareas of depigmentation in a specific pattern. The condition is commonly marked by a white depigmented patchon the scalp and forehead, observed in 80-90% of cases. Depigmentation can also extend to the eyebrows, eyelashes, and nasal root. In rare instances, hypopigmented or depigmented patches may extend to atypical sites such as the chin, anterior neck, trunk, abdomen, and limbs. This case report presents an unusual manifestation of Piebaldism, highlighting the variability of clinical manifestations associated with this genetic condition. https://pubs.sciepub.com/ajmcr/13/8/2/ajmcr-13-8-2.pdf Piebaldism Depigmentation Pediatric