Werner’s syndrome: a quite rare disease for differential diagnosis of scleroderma
Abstract
Werner’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...
Paper Details
Title
Werner’s syndrome: a quite rare disease for differential diagnosis of scleroderma
Published Date
Jun 3, 2009
Journal
Volume
30
Issue
5
Pages
695 - 698
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