Literature DB >> 19495768

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

Cemal Bes1, Seref Vardi, Melih Güven, Mehmet Soy.   

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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Year:  2009        PMID: 19495768     DOI: 10.1007/s00296-009-0982-8

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  13 in total

Review 1.  Werner's syndrome: from clinics to genetics.

Authors:  M Goto
Journal:  Clin Exp Rheumatol       Date:  2000 Nov-Dec       Impact factor: 4.473

2.  Digital ulcers in systemic sclerosis: prevention by treatment with bosentan, an oral endothelin receptor antagonist.

Authors:  J H Korn; M Mayes; M Matucci Cerinic; M Rainisio; J Pope; E Hachulla; E Rich; P Carpentier; J Molitor; J R Seibold; V Hsu; L Guillevin; S Chatterjee; H H Peter; J Coppock; A Herrick; P A Merkel; R Simms; C P Denton; D Furst; N Nguyen; M Gaitonde; Carol Black
Journal:  Arthritis Rheum       Date:  2004-12

3.  What can we learn from Werner syndrome? A biased view from a rheumatologist.

Authors:  M Goto
Journal:  Mod Rheumatol       Date:  2002-12       Impact factor: 3.023

4.  Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing.

Authors:  M Goto
Journal:  Mech Ageing Dev       Date:  1997-12       Impact factor: 5.432

5.  The spectrum of WRN mutations in Werner syndrome patients.

Authors:  Shurong Huang; Lin Lee; Nancy B Hanson; Catherine Lenaerts; Holger Hoehn; Martin Poot; Craig D Rubin; Da-Fu Chen; Chih-Chao Yang; Heike Juch; Thomas Dorn; Roland Spiegel; Elif Arioglu Oral; Mohammed Abid; Carla Battisti; Emanuela Lucci-Cordisco; Giovanni Neri; Erin H Steed; Alexa Kidd; William Isley; David Showalter; Janet L Vittone; Alexander Konstantinow; Johannes Ring; Peter Meyer; Sharon L Wenger; Axel von Herbay; Uwe Wollina; Markus Schuelke; Carin R Huizenga; Dru F Leistritz; George M Martin; I Saira Mian; Junko Oshima
Journal:  Hum Mutat       Date:  2006-06       Impact factor: 4.878

Review 6.  The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.

Authors:  Meltem Muftuoglu; Junko Oshima; Cayetano von Kobbe; Wen-Hsing Cheng; Dru F Leistritz; Vilhelm A Bohr
Journal:  Hum Genet       Date:  2008-09-23       Impact factor: 4.132

7.  Clinical, demographic, and genetic aspects of the Werner syndrome in Japan.

Authors:  M Goto; F Takeuchi; K Tanimoto; T Miyamoto
Journal:  Adv Exp Med Biol       Date:  1985       Impact factor: 2.622

8.  LMNA mutations in atypical Werner's syndrome.

Authors:  Lishan Chen; Lin Lee; Brian A Kudlow; Heloisa G Dos Santos; Olav Sletvold; Yousef Shafeghati; Eleanor G Botha; Abhimanyu Garg; Nancy B Hanson; George M Martin; I Saira Mian; Brian K Kennedy; Junko Oshima
Journal:  Lancet       Date:  2003-08-09       Impact factor: 79.321

Review 9.  Werner Syndrome, aging and cancer.

Authors:  A Ozgenc; L A Loeb
Journal:  Genome Dyn       Date:  2006

10.  Early atherosclerosis in systemic sclerosis and its relation to disease or traditional risk factors.

Authors:  Martha E Hettema; Dan Zhang; Karina de Leeuw; Ymkje Stienstra; Andries J Smit; Cees G M Kallenberg; Hendrika Bootsma
Journal:  Arthritis Res Ther       Date:  2008-04-25       Impact factor: 5.156

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  3 in total

1.  Werner's syndrome may be lost in the shadow of the scleroderma.

Authors:  Emel Gonullu; Nazife Sule Yaşar Bilge; Timuçin Kaşifoğlu; Cengiz Korkmaz
Journal:  Rheumatol Int       Date:  2012-11-06       Impact factor: 2.631

2.  Do you know this syndrome? Werner syndrome.

Authors:  Özlem Bilgiç
Journal:  An Bras Dermatol       Date:  2017 Mar-Apr       Impact factor: 1.896

3.  Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome.

Authors:  T Guastafierro; M G Bacalini; A Marcoccia; D Gentilini; S Pisoni; A M Di Blasio; A Corsi; C Franceschi; D Raimondo; A Spanò; P Garagnani; F Bondanini
Journal:  Clin Epigenetics       Date:  2017-08-30       Impact factor: 6.551

  3 in total

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