| Literature DB >> 26943360 |
H Ott1,2, C Eich3, K Schriek4,5, B Ludwikowski4,5.
Abstract
Hereditary epidermolysis bullosa (EB) represents a clinically heterogeneous group of congenital blistering disorders requiring multiprofessional care. EB is associated with a broad spectrum of potentially severe complications often reaching their full extent during school age and adolescence. This review aims at summarizing cutaneous manifestations of EB as well as extracutaneous complications of this complex disease and their interdisciplinary management.Entities:
Keywords: Adolescents; Blisters; Complications; Epidermolysis bullosa; Gastrointestinal tract; Pruritus
Mesh:
Year: 2016 PMID: 26943360 DOI: 10.1007/s00105-016-3774-6
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751