Werner's syndrome: a quite rare disease for differential diagnosis of scleroderma
Yükleniyor...
Dosyalar
Tarih
2010
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Springer Heidelberg
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
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.
Açıklama
Anahtar Kelimeler
Werner Syndrome, Scleroderma, Digital Ulcers
Kaynak
Rheumatology International
WoS Q Değeri
Q3
Scopus Q Değeri
Q2
Cilt
30
Sayı
5
