| 词条 | Laugier–Hunziker syndrome |
| 释义 |
| name = | synonym = | image = | image_size = | alt = | caption = | pronounce = | specialty = dermatology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Laugier–Hunziker syndrome ({{IPAc-en|ˈ|l|oʊ|ʒ|i|eɪ|_|ˈ|h|ʊ|n|t|s|ᵻ|k|ər}}) is a cutaneous condition characterized by hyperpigmentation of the oral mucosa,[1] longitudinal melanonychia,[1] and genital melanosis.[2] The hyperpigmentation presented in Laugier-Hunziker syndrome is benign and should be differentiated from Peutz-Jeghers syndrome. See also
References1. ^1 {{Citation |last=Nayak |first=RS |display-authors=etal |year=2012 |title=Laugier–Hunziker syndrome |journal=J Oral Maxillofac Pathol |volume=16 |issue=2 |pages=245–250 |pmid=22923898 |pmc=3424942 |doi=10.4103/0973-029X.99079 |postscript=.}} {{DEFAULTSORT:Laugier-Hunziker syndrome}}{{Dermatology-stub}}2. ^{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages= |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}} 2 : Melanocytic nevi and neoplasms|Syndromes affecting the skin |
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