Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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 Classification Disease Synonyms Adult progeria Progeria dorosłych WS WS ORPHA code 902 OMIM code 277700 ICD10 code E34.8 ICD11 code 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