Piebaldism 5070047 216248613 2008-05-31T20:10:14Z Arcadian 104523 nav {{Infobox_Disease | Name = {{PAGENAME}} | Image = | Caption = | DiseasesDB = 29295 | ICD10 = {{ICD10|E|70|3|e|70}} ([[ILDS]] E70.350) | ICD9 = {{ICD9|709.09}} | ICDO = | OMIM = 172800 | MedlinePlus = | eMedicineSubj = derm | eMedicineTopic = 689 | MeshID = D016116 | }} '''Piebaldism''' is a rare [[Mendelian inheritance|autosomal dominant]] disorder of [[melanocyte]] development. Common characteristics include a congenital white forelock, scattered normal pigmented and hyperpigmented [[macule|macules]] and a triangular shaped depigmented patch on the forehead. Although piebaldism can be classed as partial [[albinism]] the vision problems associated with albinism are not usually present as eye pigmentation is normal. ==External links== * {{DermAtlas|874885248}} {{disease-stub}} {{Amino acid metabolic pathology}} {{Diseases of the skin and subcutaneous tissue}} [[de:Piebaldismus]] [[fr:PiƩbaldisme]] [[pl:Piebaldyzm]]