Epidermolysis bullosa. Part 1: causes, presentation and complications
- 1 March 2008
- journal article
- review article
- Published by Mark Allen Group in British Journal of Nursing
- Vol. 17 (5) , 292-296
- https://doi.org/10.12968/bjon.2008.17.5.28824
Abstract
This article is the first in a series of three focusing on the causes, clinical presentation, complications and care of adult patients affected by epidermolysis bullosa (EB), a group of rare genetic skin fragility disorders. Although the condition is rare, in some cases it presents extreme challenges both to those affected and those involved in the care of the EB patient; therefore, these articles may have relevance for other long-term disorders. While there is a wealth of information regarding the ‘science’ of EB there is dearth of information regarding the care of the adult EB patient, and this series of articles will endeavour to fill that gap. This article focuses mainly on those patients affected with the most severe form of EB found in the adult group, recessive dystrophic epidermolysis bullosa; with the part two looking at the care of the adult with EB from the nursing perspective, including wound management, and the experiences of a specialist EB psychotherapist being presented in the final article of the series. Readers will thus have an opportunity to gain an overall view of this difficult condition.Keywords
This publication has 25 references indexed in Scilit:
- Esophageal strictures in children with recessive dystrophic epidermolysis bullosa: an 11-year experience with fluoroscopically guided balloon dilatationJournal of Pediatric Surgery, 2006
- Bone mineralization in children with epidermolysis bullosaBritish Journal of Dermatology, 2006
- Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis Bullosa: Experience of the National Epidermolysis Bullosa Registry, 1986–2002Journal of Hand Surgery (European Volume), 2005
- GENITOURINARY COMPLICATIONS OF INHERITED EPIDERMOLYSIS BULLOSA: EXPERIENCE OF THE NATIONAL EPIDERMYLOSIS BULLOSA REGISTRY AND REVIEW OF THE LITERATUREJournal of Urology, 2004
- Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosaClinical and Experimental Dermatology, 2004
- Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosaJournal of the American Academy of Dermatology, 2000
- Recessive dystrophic epidermolysis bullosa complicated with nephrotic syndrome due to secondary amyloidosisInternational Journal of Dermatology, 2000
- Diagnostic dilemma of “sporadic” cases of dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?Experimental Dermatology, 1999
- Gastrostomy and growth in dystrophic epidermolysis bullosaBritish Journal of Dermatology, 1996
- The anaesthetic management of patients with dystrophic epidermolysis bullosaAnaesthesia, 1993