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Familial generalized lentiginosis
rareFamilial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.
- Identifiers
- MONDO:0007891 OMIM:151001Orphanet:231040
- Part of
- Hyperpigmentation of the skin
- Also known as
- familial lentigines profusa · familial multiple lentigines syndrome without systemic involvement · lentiginosis, generalised
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