PiebaldismÂ?‚ is a rareÂ?‚ autosomal dominantÂ?‚ disorder ofÂ?‚ melanocyteÂ?‚ development. Common characteristics include a congenital whiteÂ?‚ forelock, scattered normal pigmented and hypo pigmentedÂ?‚ maculesÂ?‚ and a triangular shaped depigmented patch on the forehead.In some cases, piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung’s disease. Primary melanocytes isolated from a patient with piebaldism can be used as a tool […]
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