Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders. Disease data Klasyfikacja Disease Synonimy Adult progeria Progeria dorosłych WS WS Kod ORPHA 902 Kod OMIM 277700 Kod ICD10 E34.8 Kod ICD11 LD2B *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