Literature DB >> 14672683

Chronic leg ulcers in Werner's syndrome.

E K Yeong1, C C Yang.   

Abstract

We report two siblings suffered from Werner's syndrome, which is a rare premature aging disorder caused by genetic mutations. They developed premature aging during adolescence with loss and graying of hair, short stature, baldness, atrophic skin, thin extremities, flat feet, 'bird' face and cataracts. Multiple chronic ulcers were noted over the feet in both patients. Healing was prolonged because of atrophic subcutaneous tissue, poor perfusion, impaired fibroblast activity and the loss of normal foot architecture. Treatment of the ulcers was challenging, as flap options were limited over the lower third of the leg and skin grafting was not easy as there was a lack of healthy granulations. However, we have successfully closed the ulcers with Integra artificial skin and ultra-thin split thickness skin grafting with the scalp as donor site. The main purpose of this paper is to alert physicians to this syndrome when treatments are being planned for patients with chronic leg ulcers.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14672683     DOI: 10.1016/j.bjps.2003.10.011

Source DB:  PubMed          Journal:  Br J Plast Surg        ISSN: 0007-1226


  11 in total

1.  Clinical utility gene card for: Werner syndrome.

Authors:  Fuki M Hisama; Christian Kubisch; George M Martin; Junko Oshima
Journal:  Eur J Hum Genet       Date:  2012-01-18       Impact factor: 4.246

2.  A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies.

Authors:  Ruben Agrelo; Miguel Arocena Sutz; Fernando Setien; Fabian Aldunate; Manel Esteller; Valeria Da Costa; Ricardo Achenbach
Journal:  Epigenetics       Date:  2015       Impact factor: 4.528

Review 3.  Cellular senescence: a view throughout organismal life.

Authors:  Cayetano von Kobbe
Journal:  Cell Mol Life Sci       Date:  2018-07-20       Impact factor: 9.261

4.  Clinical utility gene card for: Werner Syndrome--Update 2014.

Authors:  Fuki M Hisama; Christian Kubisch; George M Martin; Junko Oshima
Journal:  Eur J Hum Genet       Date:  2014-09-03       Impact factor: 4.246

Review 5.  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

Review 6.  Skin Abnormalities in Disorders with DNA Repair Defects, Premature Aging, and Mitochondrial Dysfunction.

Authors:  Mansoor Hussain; Sudarshan Krishnamurthy; Jaimin Patel; Edward Kim; Beverly A Baptiste; Deborah L Croteau; Vilhelm A Bohr
Journal:  J Invest Dermatol       Date:  2021-01-19       Impact factor: 8.551

Review 7.  Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming.

Authors:  Akira Shimamoto; Koutaro Yokote; Hidetoshi Tahara
Journal:  Front Genet       Date:  2015-01-29       Impact factor: 4.599

8.  Physician-initiated clinical study of limb ulcers treated with a functional peptide, SR-0379: from discovery to a randomized, double-blind, placebo-controlled trial.

Authors:  Hironori Nakagami; Ken Sugimoto; Takahiro Ishikawa; Taku Fujimoto; Toshifumi Yamaoka; Misa Hayashi; Eiji Kiyohara; Hiroshi Ando; Yuta Terabe; Yoichi Takami; Koichi Yamamoto; Yasushi Takeya; Minoru Takemoto; Masaya Koshizaka; Tamotsu Ebihara; Ayumi Nakamura; Mitsunori Nishikawa; Xiang Jing Yao; Hideki Hanaoka; Ichiro Katayama; Koutaro Yokote; Hiromi Rakugi
Journal:  NPJ Aging Mech Dis       Date:  2018-02-13

9.  Novel Surgical Treatment for Refractory Heel Ulcers in Werner's Syndrome.

Authors:  Keisuke Oe; Masahiko Miwa; Yoshitada Sakai; Masahiro Kurosaka
Journal:  Case Rep Orthop       Date:  2013-08-26

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.