Literature DB >> 18414291

Epidermolysis bullosa. Part 1: causes, presentation and complications.

Elizabeth Pillay1.   

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.

Entities:  

Mesh:

Year:  2008        PMID: 18414291     DOI: 10.12968/bjon.2008.17.5.28824

Source DB:  PubMed          Journal:  Br J Nurs        ISSN: 0966-0461


  7 in total

Review 1.  Living in dressings and bandages: findings from workshops with people with Epidermolysis bullosa.

Authors:  Patricia Grocott; Rebecca Blackwell; Heather Weir; Elizabeth Pillay
Journal:  Int Wound J       Date:  2012-04-04       Impact factor: 3.315

2.  Dental and Anaesthetic Challenges in a Patient with Dystrophic Epidermolysis Bullosa.

Authors:  Ali Al-Abadi; Salah A Al-Azri; Abdulaziz Bakathir; Yusra Al-Riyami
Journal:  Sultan Qaboos Univ Med J       Date:  2016-11-30

3.  Bone marrow transplant with post-transplant cyclophosphamide for recessive dystrophic epidermolysis bullosa expands the related donor pool and permits tolerance of nonhaematopoietic cellular grafts.

Authors:  C L Ebens; J A McGrath; K Tamai; A Hovnanian; J E Wagner; M J Riddle; D R Keene; T E DeFor; R Tryon; M Chen; D T Woodley; K Hook; J Tolar
Journal:  Br J Dermatol       Date:  2019-06-28       Impact factor: 9.302

4.  Bone marrow transplantation for recessive dystrophic epidermolysis bullosa.

Authors:  John E Wagner; Akemi Ishida-Yamamoto; John A McGrath; Maria Hordinsky; Douglas R Keene; David T Woodley; Mei Chen; Megan J Riddle; Mark J Osborn; Troy Lund; Michelle Dolan; Bruce R Blazar; Jakub Tolar
Journal:  N Engl J Med       Date:  2010-08-12       Impact factor: 91.245

Review 5.  Novel and emerging therapies in the treatment of recessive dystrophic epidermolysis bullosa.

Authors:  Ellie Rashidghamat; John A McGrath
Journal:  Intractable Rare Dis Res       Date:  2017-02

Review 6.  Co-producing novel wound care products for Epidermolysis bullosa; an empirical case study of the use of surrogates in the design and prototype development process.

Authors:  Patricia Grocott; Rebecca Blackwell; Conchita Currie; Elizabeth Pillay; Glenn Robert
Journal:  Int Wound J       Date:  2012-04-09       Impact factor: 3.315

Review 7.  A review of the obstetric management of patients with epidermolysis bullosa.

Authors:  L A Bolt; G O'Sullivan; D Rajasingham; A Shennan
Journal:  Obstet Med       Date:  2010-09-17
  7 in total

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