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Epidermolysis Bullosa Simplex


Authors: H. Bučková 1;  J. Buček 2
Authors‘ workplace: Dětské kožní oddělení, FN Brno - Dětská nemocnice 1
Published in: Čes-slov Pediat 2000; (8): 498-501.
Category:

Overview

Epidermolysis bullosa simplex (EBS) belongs into the group of inborn mechanobullous diseases mostly withan autosomal dominant inheritance. The development of the clinical picture, correct collection of a new blister andexperience with the histological diagnosis incl. electron microscopy are the basis for correct diagnosis. Patients, inparticular those with the localized form of epidermolysis bullosa simplex frequentl y escape the attention of doctors.The authors discuss their own experience with the diagnosis of 18 patients with EBS.

Key words:
epidermolysis bullosa simplex, clinical picture, electron microscopy, concentration of patients into

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Labels
Neonatology Paediatrics General practitioner for children and adolescents
Topics Journals
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