Junctional epidermolysis bullosa: a case report
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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
1Department of Paediatric and Community Dentistry, Philipps-University Marburg, Marburg, Germany. momeni@mailer.uni-marburg.de
Abstract:
Epidermolysis bullosa (EB) is a group of genetically determined disorders characterized by blistering of the skin and mucosae. There are three major forms--simple, junctional and dystrophic--and each has several varieties. The present case report describes a male child with junctional EB. The aim of the report is to present the dietary situation and the dental status of the child, examples of potential dental and nutritional consequences, and the therapeutic interventions possible for children with this disease.
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