Familial generalized lentiginosis

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Synonyms: Familial lentigines profusa | Familial multiple lentigines syndrome without systemic involvement

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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Familial generalized lentiginosis?

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Clinical Trials

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