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
1984 ◽  
Vol 21 (2) ◽  
pp. 191-197 ◽  
Author(s):  
Carlomaurizio Montecucco ◽  
Giuseppe Attardo-Parrinello ◽  
Giuseppe Brambilla ◽  
Enrico L. Chérié-Lignière ◽  
Edoardo Ascari

2009 ◽  
Vol 2009 ◽  
pp. 1-3 ◽  
Author(s):  
Murat Sert ◽  
Koray Fakioglu ◽  
Tamer Tetiker

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.


2011 ◽  
Vol 50 (3) ◽  
pp. 347-349
Author(s):  
Orlando Cedeno ◽  
Kaj Klaue ◽  
Valerie Cohen

1991 ◽  
Vol 21 (2) ◽  
pp. 135-142 ◽  
Author(s):  
Hiroyuki Tsuchiya ◽  
Katsuro Tomita ◽  
Masaaki Ohno ◽  
Makoto Inaoki ◽  
Atsuhiro Kawashima

2018 ◽  
Vol 9 (2) ◽  
pp. 148-151
Author(s):  
Farhana Tahseen Taj ◽  
Divya Vupperla ◽  
Sridevi Raichur ◽  
Jolika Ardeshana

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Chun-li Chen ◽  
Jia-song Yang ◽  
Xiang Zhang ◽  
Tian Tian ◽  
Rui Zeng ◽  
...  

Gerontology ◽  
2002 ◽  
Vol 48 (4) ◽  
pp. 215-219 ◽  
Author(s):  
Tomohiro Nakayama ◽  
Toyoko Ochiai ◽  
Yoshiko Takahashi ◽  
Kimie Ohkubo ◽  
Takashi Hironaga ◽  
...  

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