Beş, CemalVardı, ŞerefGüven, MelihSoy, Mehmet2021-06-232021-06-2320100172-81721437-160Xhttps://doi.org/10.1007/s00296-009-0982-8https://hdl.handle.net/20.500.12491/6742Werner's syndrome (WS) is an autosomal recessive disorder characterized by premature aging. The main features of the disease are scleroderma-like skin appearance, premature atherosclerosis, short stature, diabetes mellitus, early osteoporosis and early aging. Herein, we describe a patient with WS, who has scleroderma-like skin changes and discuss the literature about WS as a disease in the differential diagnosis of systemic sclerosis.eninfo:eu-repo/semantics/closedAccessWerner SyndromeSclerodermaDigital UlcersArticle10.1007/s00296-009-0982-8305695698194957682-s2.0-77951023059Q2WOS:000274634400022Q3