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Laugier–Hunziker syndrome

Medical condition From Wikipedia, the free encyclopedia

Laugier–Hunziker syndrome
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Laugier–Hunziker syndrome (/ˈlʒi ˈhʊntsɪkər/) is a cutaneous condition characterized by hyperpigmentation of the oral mucosa,[1] longitudinal melanonychia,[1] and genital melanosis.[2]

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The hyperpigmentation presented in Laugier-Hunziker syndrome is benign and should be differentiated from Peutz-Jeghers syndrome.

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