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Piebaldism
rarePiebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes.
- Identifiers
- MONDO:0008244 OMIM:172800Orphanet:2884
- Causal genes
- KIT
- Part of
- Autosomal dominant diseaseEye disorderHereditary skin disorderHypopigmentation of the skinNeurocristopathy
- Also known as
- PBT · piebald trait
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