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
Labels
Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
2000 Issue 8
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