44 2033180199
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Department of Diagnostic Sciences and Oral Biology, King Khalid University, Kingdom of Saudi Arabia


  • Case Reports   
    Laugier-Hunziker syndrome: a rare case report
    Author(s): Saeed Arem*

    Pigmented disorders were commonly encountered in the oral cavity, varying from a focal to diffuse presentation with the varied etiological causes ranging from the exogenous to endogenous sources. Laugier-Hunziker syndrome is a rare, hereditary pigmentary disorder characterized by mucocutaneous lentiginous lesions and melanonychia. It is regarded as a diagnosis of exclusion. Here we present a case of a 70-year female with uncommon intra and extra oral pigmentation along with the melanonychia who was diagnosed with Laugier-Hunziker syndrome. Careful examination of other disorders causing the similar pigmentation has to be carefully evaluated before arriving at a final diagnosis.. Read More»
    DOI: 10.37532. puldcr-

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Citations : 232

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