These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Laugier-Hunziker syndrome: a report of three cases and literature review.
    Author: Wang WM, Wang X, Duan N, Jiang HL, Huang XF.
    Journal: Int J Oral Sci; 2012 Dec; 4(4):226-30. PubMed ID: 23174847.
    Abstract:
    Laugier-Hunziker syndrome (LHS) is an acquired pigmentary condition affecting lips, oral mucosa and acral area, frequently associated with longitudinal melanonychia. There is neither malignant predisposition nor underlying systemic abnormality associated with LHS. Herein, we present three uncommon cases of LHS with possibly new feature of nail pigmentation, which were diagnosed during the past 2 years. We also review the clinical and histological findings, differential diagnosis, and treatment of the syndrome in published literature.
    [Abstract] [Full Text] [Related] [New Search]