Literature DB >> 9155958

The prevalence of epidermolysis bullosa in Scotland.

H M Horn1, G C Priestley, R A Eady, M J Tidman.   

Abstract

The prevalence of epidermolysis bullosa (EB) in Britain and most other countries is unknown. Patients suffering from the inherited forms of EB and living in Scotland have been traced. Two hundred and fifty-nine affected people from 76 families have been identified, of whom 211 were clinically assessed. One-third of these Scottish EB sufferers had never been seen by a dermatologist. In Lothian, where there appears to be a relatively high prevalence of EB, 75% of patients were unknown to their general practitioners. The point prevalence of all forms of EB at the outset of the study was 49.0 per million, comprising EB simplex 28.6 per million and dystrophic EB 20.4 per million. Extrapolation of accurate data available for the Lothians suggests that the point prevalence of all forms of EB in Scotland is in excess of these figures.

Entities:  

Mesh:

Year:  1997        PMID: 9155958

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  13 in total

1.  Rare case of dysphagia, skin blistering, missing nails in a young boy.

Authors:  Jasbir Makker; Bharat Bajantri; Prospere Remy
Journal:  World J Gastrointest Endosc       Date:  2015-02-16

2.  Psychiatric symptoms and quality of life in patients affected by epidermolysis bullosa.

Authors:  Francesco Margari; Paola A Lecce; Wanda Santamato; Patrizia Ventura; Nicola Sportelli; Giuseppina Annicchiarico; Ernesto Bonifazi
Journal:  J Clin Psychol Med Settings       Date:  2010-12

3.  Autosomal recessive inheritance of a novel missense mutation of ITGB4 for Epidermolysis-Bullosa pyloric-atresia: a case report.

Authors:  Suman Kalyan Paine; Subrata Das; Chandrika Bhattacharyya; Nidhan Kumar Biswas; Raghavendra Rao; Abhishek De; Analabha Basu
Journal:  Mol Genet Genomics       Date:  2022-08-23       Impact factor: 2.980

Review 4.  Anesthetic Management of Adults With Epidermolysis Bullosa.

Authors:  Brita M Mittal; Candida L Goodnough; Erin Bushell; Sophia Turkmani-Bazzi; Kelly Sheppard
Journal:  Anesth Analg       Date:  2022-01-01       Impact factor: 6.627

Review 5.  Inherited epidermolysis bullosa.

Authors:  Jo-David Fine
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

6.  From Clinical Phenotype to Genotypic Modelling: Incidence and Prevalence of Recessive Dystrophic Epidermolysis Bullosa (RDEB).

Authors:  Shaundra Eichstadt; Jean Y Tang; Daniel C Solis; Zurab Siprashvili; M Peter Marinkovich; Nedra Whitehead; Matthew Schu; Fang Fang; Stephen W Erickson; Mary E Ritchey; Max Colao; Kaye Spratt; Amir Shaygan; Mark J Ahn; Kavita Y Sarin
Journal:  Clin Cosmet Investig Dermatol       Date:  2019-12-24

7.  A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.

Authors:  Andrew J Cassidy; Maurice A M van Steensel; Peter M Steijlen; Michel van Geel; Jaap van der Velden; Susan M Morley; Alessandro Terrinoni; Gerry Melino; Eleonora Candi; W H Irwin McLean
Journal:  Am J Hum Genet       Date:  2005-10-11       Impact factor: 11.025

Review 8.  Dystrophic epidermolysis bullosa: a review.

Authors:  Satoru Shinkuma
Journal:  Clin Cosmet Investig Dermatol       Date:  2015-05-26

9.  Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?

Authors:  R Baardman; V K Yenamandra; J C Duipmans; A M G Pasmooij; M F Jonkman; P C van den Akker; M C Bolling
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-11-16       Impact factor: 6.166

10.  Death from colonic disease in epidermolysis bullosa dystrophica.

Authors:  Chih-Hsin Hsieh; Che-Jen Huang; Gau-Tyan Lin
Journal:  BMC Dermatol       Date:  2006-02-15
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