scholarly journals Werner’s syndrome: A case report and review of literature

2018 ◽  
Vol 9 (2) ◽  
pp. 148-151
Author(s):  
Farhana Tahseen Taj ◽  
Divya Vupperla ◽  
Sridevi Raichur ◽  
Jolika Ardeshana
Keyword(s):  
Case Report ◽  
Review Of Literature ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

Werner's Syndrome Combined with Quintuplicate Malignant Tumors: A Case Report and Review of Literature Data

1991 ◽  
Vol 21 (2) ◽  
pp. 135-142 ◽  
Author(s):  
Hiroyuki Tsuchiya ◽  
Katsuro Tomita ◽  
Masaaki Ohno ◽  
Makoto Inaoki ◽  
Atsuhiro Kawashima
Keyword(s):  
Case Report ◽  
Malignant Tumors ◽  
Review Of Literature ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

Improvement of hyperinsulinemic diabetes following removal of a meningioma in werner’s syndrome. A case report

1984 ◽  
Vol 21 (2) ◽  
pp. 191-197 ◽  
Author(s):  
Carlomaurizio Montecucco ◽  
Giuseppe Attardo-Parrinello ◽  
Giuseppe Brambilla ◽  
Enrico L. Chérié-Lignière ◽  
Edoardo Ascari
Keyword(s):  
Case Report ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

scholarly journals A Case Report of Werner’s Syndrome With a Novel Mutation From India

Cureus ◽  
2020 ◽  
Author(s):  
Ajeet Singh ◽  
Satyaki Ganguly ◽  
Namrata Chhabra ◽  
Hitesh Yadav ◽  
Junko Oshima
Keyword(s):  
Case Report ◽  
Novel Mutation ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

scholarly journals Review of Two Siblings with Werner's Syndrome: A Case Report

2009 ◽  
Vol 2009 ◽  
pp. 1-3 ◽  
Author(s):  
Murat Sert ◽  
Koray Fakioglu ◽  
Tamer Tetiker
Keyword(s):  
Diabetes Mellitus ◽  
Case Report ◽  
Clinical Course ◽  
Initial Diagnosis ◽  
Werner’S Syndrome ◽  
Gray Hair ◽  
Werner's Syndrome ◽  
Renal Parenchymal Disease ◽  
Parenchymal Disease

We report the clinical course of two siblings with Werner's syndrome (WS) who were diagnosed and followed at our clinics for 12 years. Initial diagnosis of the first sibling (sister) was at age 20, the second (brother) at 16. At the initial diagnosis, the sister had amenorrhea, muscle atrophy at arms and legs, diabetes mellitus (DM), short stature, bilateral cataracts, genital hypoplasia, osteoporosis, and gray hair. During 12 years follow-up period, high-pitched voice, hepatosteatosis, renal parenchymal disease, and urethral obstruction developed. Regarding the brother, DM, cataracts and genital hypoplasia were observed at the initial diagnosis. During the 12 years follow-up period, gray hair, high-pitched voice, steatohepatosis, and osteoporosis developed.

A Complex Forefoot Malunion in a Patient with Werner’s Syndrome: A Case Report

2011 ◽  
Vol 50 (3) ◽  
pp. 347-349
Author(s):  
Orlando Cedeno ◽  
Kaj Klaue ◽  
Valerie Cohen
Keyword(s):  
Case Report ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

scholarly journals A case report of Werner’s syndrome with bilateral juvenile cataracts

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Chun-li Chen ◽  
Jia-song Yang ◽  
Xiang Zhang ◽  
Tian Tian ◽  
Rui Zeng ◽  
...  
Keyword(s):  
Case Report ◽  
Werner’S Syndrome ◽  
Werner's Syndrome

scholarly journals RARE CASE REPORT: WERNER’S SYNDROME - PREMATURE AGING SYNDROME SEEN IN TWO SISTERS

2013 ◽  
Vol 2 (45) ◽  
pp. 8864-8868
Author(s):  
Gopal M.G. ◽  
Kavya Raju Nayak ◽  
Sharath Kumar B.C ◽  
Ramesh M ◽  
Nandini A.S
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Premature Aging ◽  
Werner’S Syndrome ◽  
Werner's Syndrome ◽  
Rare Case Report ◽  
Premature Aging Syndrome
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