Familial generalized lentiginosis

Familial 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.

Also known as: familial lentigines profusa, familial multiple lentigines syndrome without systemic involvement, lentiginosis profusa, lentiginosis, diffuse, lentiginosis, generalised, lentiginosis, generalized, lentiginosis, inherited patterned

8 clinical trials for this condition and its sub-types.