WERNER-SYNDROME

Authors
Citation
M. Duvic et Na. Lemak, WERNER-SYNDROME, Dermatologic clinics, 13(1), 1995, pp. 163-168
Citations number
NO
Categorie Soggetti
Dermatology & Venereal Diseases
Journal title
ISSN journal
07338635
Volume
13
Issue
1
Year of publication
1995
Pages
163 - 168
Database
ISI
SICI code
0733-8635(1995)13:1<163:W>2.0.ZU;2-C
Abstract
Patients with Werner's syndrome almost invariably have disorders of th e skin or its appendages; therefore, dermatologists should be aware of the typical clincial picture. Characteristic features include short s tature with slender limbs and stocky trunk; growth arrested at puberty ; thin, sparse, prematurely gray hair; cataracts appearing in patients in their 20s and 30s; shiny, taut skin with ulcers of feet and legs; hyperkeratotic calluses; endocrine abnormalities; and increased likeli hood of neoplasms among patients and their families. The probability o f the appearance of this autosomal recessive disease is increased by c onsanguineous marriage. The life span of patients is shortened, and de ath usually results from vascular disease or malignancy.