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Lipoid Proteinosis in two Iranian Sisters: A Case Report and Review of Literature

AUTHORS

F Malekzad 1 , H Rahimi 2 , * , S Lotfi 1 , M Qaisari 1

AUTHORS INFORMATION

1 Department of Dermatology, Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

2 Department of Dermatology, Skin Research Center, Shahid Beheshti University of Medical Sciences, MC Shohada-e Tajrish Hospital, Shahrdari St, 1989934148, hoda_rahimi@yahoo.com, Tehran, Iran

How to Cite: Malekzad F, Rahimi H, Lotfi S, Qaisari M. Lipoid Proteinosis in two Iranian Sisters: A Case Report and Review of Literature, Iran Red Crescent Med J. Online ahead of Print ; 13(4):280-282.

ARTICLE INFORMATION

Iranian Red Crescent Medical Journal: 13 (4); 280-282
Article Type: Case Report
Received: August 10, 2010
Accepted: October 18, 2010

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Abstract

Lipoid proteinosis is a rare autosomal recessive disorder which may be seen within a family very occasionally. Herein, we report lipoid proteinosis in two sisters characterized by verrucous lesions and hoarseness of voice, dysphagia and multiple beaded papules along the margins of their eyelids, fissured lips and thick ferenulum.

Keywords

Lipoid proteinosis Urbach-Weithe disease Hyalinosis cutis et mucosa

© 0, Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

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