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GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA

A Journal on Dermatology and Sexually Transmitted Diseases


Official Journal of the Italian Society of Dermatology and Sexually Transmitted Diseases
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Giornale Italiano di Dermatologia e Venereologia 2018 February;153(1):111-4

DOI: 10.23736/S0392-0488.16.04887-2

Copyright © 2015 EDIZIONI MINERVA MEDICA

language: English

Kindler syndrome: the case of two Iranian sisters

Saeed KARGAR 1, Seyed M. SHIRYAZDI 1 , Hossein NEAMATZADEH 2, 3, Vahid RAMAZANI 4

1 Department of General Surgery, Shahid Sadoughi Hospital, Shahid Sadoughi University of Medical Sciences, Yazd, Iran; 2 Department of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran; 3 Mother and Newborn Health Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran; 4 Islamic Azad University, Ashkzar Branch, Ashkzar, Yazd, Iran


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Kindler syndrome is a rare autosomal recessive condition, characterized by multiple skin and mucosal abnormalities. Among the latter, esophageal involvement is an infrequent manifestation which may be completely asymptomatic or complicated by dysphagia. We report the case of two sisters presenting with cutaneous features and severe dysphagia. Endoscopic examination showed that the patients were affected by a rare condition named “esophageal web”. Both patients showed significant improvement after balloon dilation. Clinicians should be aware of the potential complications of this disease, and the approach by balloon dilation should be considered as primary therapy in Kindler syndrome patients with esophageal web.


KEY WORDS: Poikiloderma of Kindler - Esophagus - Esophageal web - Epidermolysis bullosa

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Publication History

Issue published online: January 8, 2018
Article first published online: July 8, 2016
Manuscript accepted: March 20, 2015
Manuscript revised: February 26, 2015
Manuscript received: July 20, 2014

Cite this article as

Kargar S, Shiryazdi SM, Neamatzadeh H, Ramazani V. Kindler syndrome: the case of two Iranian sisters. G Ital Dermatol Venereol 2018;153:111-4. DOI: 10.23736/S0392-0488.16.04887-2

Corresponding author e-mail

smshiryazdi@yahoo.com