Laugier–Hunziker syndrome
Laugier–Hunziker syndrome | |
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Specialty | Dermatology |
Laugier–Hunziker syndrome (/ˈloʊʒieɪ ˈhʊntsɪkər/) 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[]
- Peutz–Jeghers syndrome
- List of cutaneous conditions
References[]
Categories:
- Melanocytic nevi and neoplasms
- Syndromes affecting the skin
- Dermatology stubs