Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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. Disease data Classification Disease Synonyms Familial lentigines profusa Rodzinny zespół mnogich plam soczewicowatych Familial multiple lentigines syndrome without systemic involvement ORPHA code 231040 OMIM code 151001 ICD10 code L81.4 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl