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Сімейний генералізований лентигіноз

ORPHA:231040· ICD-10 L81.4· Familial generalized lentiginosis

Визначення(English summary)

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.

Поширеність
Unknown
Успадкування
Autosomal dominant, Unknown
Вік початку
All ages