Laugier–Hunziker syndrome
Laugier–Hunziker syndrome (/ˈloʊʒieɪ ˈhʊntsɪkər/) is a cutaneous condition characterized by hyperpigmentation of the oral mucosa,[1] longitudinal melanonychia,[1] and genital melanosis.[2]
| Laugier–Hunziker syndrome | |
|---|---|
 | |
| Specialty | Dermatology |
The hyperpigmentation presented in Laugier-Hunziker syndrome is benign and should be differentiated from Peutz-Jeghers syndrome.
See also
- Peutz–Jeghers syndrome
- List of cutaneous conditions
References
- Nayak, RS; et al. (2012), "Laugier–Hunziker syndrome", J Oral Maxillofac Pathol, 16 (2): 245–250, doi:10.4103/0973-029X.99079, PMC 3424942, PMID 22923898.
- Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.