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The clinical spectrum of dystrophic epidermolysis bullosa
Author(s) -
Horn H.M.,
Tidman M.J.
Publication year - 2002
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1046/j.1365-2133.2002.04607.x
Subject(s) - genodermatosis , medicine , dermatology , epidermolysis bullosa , dysphagia , population , epidermolysis bullosa dystrophica , hyperhidrosis , constipation , palmoplantar keratoderma , genetic disorder , surgery , genetics , hyperkeratosis , gene , disease , biology , environmental health
Summary Background Dystrophic epidermolysis bullosa (DEB) is a genodermatosis resulting from mutations in COL7A1 , the gene encoding type VII collagen. The site and specific nature of the underlying mutation determine the clinical phenotype, which ranges widely from a severe mutilating condition to a relatively mild disorder. Objectives To document the clinical spectrum of DEB within a defined complete population. Methods Since 1992, when compilation of the U.K. epidermolysis bullosa register began, an exhaustive search for DEB sufferers within the Scottish population has been undertaken and their clinical features comprehensively recorded. Results One hundred and twenty‐eight DEB sufferers have been identified within the Scottish population. In descending order, the frequencies of the different forms of DEB were dominant DEB (DDEB) in 88 individuals (68%), DEB of uncertain inheritance in 24 (19%) and recessive DEB (RDEB) in 16 patients (13%). Within this latter group, nine (7%) had the mutilating Hallopeau–Siemens subtype (RDEB‐HS), five (4%) had localized (RDEB‐loc) and two (2%) had a predominantly flexural (inverse) form of RDEB. During the study, two patients with RDEB died from squamous cell carcinomas (SCCs), one originating in the skin and the second arising in the oesophagus. Gastrointestinal problems such as dysphagia, constipation and anal fissures, and restriction of mouth opening were experienced by the majority of patients with RDEB and by a significant minority of DDEB sufferers. Pseudosyndactyly was most severe in RDEB‐HS, all those over 9 years of age having mitten deformities of the hands. Milder pseudosyndactyly or flexion contractures of the fingers were present in younger patients with this subtype, in most adults suffering from other subtypes of RDEB and in 6% of those with DDEB. External ear involvement, a feature not often reported in DEB, was common in RDEB and also occurred in a minority of those with DDEB. Pruriginous lesions and albopapuloid lesions were each present in both DDEB and RDEB. Conclusions Most patients with DEB have relatively mild dominantly inherited disease, only a minority suffering from severe recessive subtypes. Scarring, gastrointestinal involvement, albopapuloid lesions and a pruriginosa‐like pattern each occur in both DDEB and RDEB. With increasing age, SCC is a major cause of morbidity and mortality.