Piebaldism

Piebaldism

Infobox_Disease
Name = PAGENAME


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 autosomal dominant disorder of melanocyte development. Common characteristics include a congenital white forelock, scattered normal pigmented and hyperpigmented 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.

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  • piebaldism — Patchy absence of the pigment of scalp hair, giving a streaked appearance; patches of vitiligo may be present in other areas due to absence of melanocytes; often transmitted as an autosomal dominant trait caused by mutation in the KIT …   Medical dictionary

  • piebaldism — noun A rare autosomal dominant disorder of melanocyte development, whose common characteristics include a congenital white forelock, scattered normally pigmented and hyperpigmented macules, and a triangular depigmented patch on the forehead …   Wiktionary

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