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

Publications

• 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-22.6.5.16-18

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