Volume 58, Issue 1 (6 2000)                   Tehran Univ Med J 2000, 58(1): 104-108 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Seirafi H, Farnaghi F, Ghani Nezhad H. Kindler syndrome and Epidermolysis Bullosa Simplex: Report of three cases. Tehran Univ Med J 2000; 58 (1) :104-108
URL: http://tumj.tums.ac.ir/article-1-1431-en.html
Abstract:   (6222 Views)

Kindler syndrome is characterized by acral blister formation in infancy and childhood, poikiloderma and cutaneous atrophy. Undoubtedly, similarities of the clinical features exist between Kindler syndrome and Epidermolysis bullosa simplex with mottled pigmentation. In this article, we report 3 patients with Kindler syndrome. Until the Bullous component of Kindler syndrome is more completely understood, we believe that this disorder should continue to be classified as a separate disease.

Full-Text [PDF 998 kb]   (1452 Downloads)    

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 , Tehran University of Medical Sciences, CC BY-NC 4.0

Designed & Developed by : Yektaweb