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Published in: Rheumatology International 5/2010

01-03-2010 | Case Report

Werner’s syndrome: a quite rare disease for differential diagnosis of scleroderma

Authors: Cemal Bes, Şeref Vardı, Melih Güven, Mehmet Soy

Published in: Rheumatology International | Issue 5/2010

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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 sclerosis.
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Metadata
Title
Werner’s syndrome: a quite rare disease for differential diagnosis of scleroderma
Authors
Cemal Bes
Şeref Vardı
Melih Güven
Mehmet Soy
Publication date
01-03-2010
Publisher
Springer-Verlag
Published in
Rheumatology International / Issue 5/2010
Print ISSN: 0172-8172
Electronic ISSN: 1437-160X
DOI
https://doi.org/10.1007/s00296-009-0982-8

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