Literature DB >> 29679399

Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes.

Cristina Has1, Judith Fischer2.   

Abstract

Inherited epidermolysis bullosa (EB) is a group of heterogeneous genetic disorders characterized by skin fragility. EB comprises a large spectrum of phenotypes, ranging from severe cutaneous and extracutaneous involvement caused by lack of key adhesion proteins, to mild cutaneous fragility caused by subtle molecular defects. Disease-causing variants in 20 different genes account for the genetic and allelic heterogeneity of EB. Here, we discuss the development of laboratory methods that enabled these discoveries and the clinical and molecular features of some new EB entities elucidated during the past 5-6 years.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  blistering; epidermal adhesion; epidermolysis bullosa; genodermatosis; mutation

Year:  2018        PMID: 29679399     DOI: 10.1111/exd.13668

Source DB:  PubMed          Journal:  Exp Dermatol        ISSN: 0906-6705            Impact factor:   3.960


  15 in total

Review 1.  Organization, dynamics and mechanoregulation of integrin-mediated cell-ECM adhesions.

Authors:  Pakorn Kanchanawong; David A Calderwood
Journal:  Nat Rev Mol Cell Biol       Date:  2022-09-27       Impact factor: 113.915

2.  Eye Involvement and Management in Inherited Epidermolysis Bullosa.

Authors:  Yasmine Bachir; Alejandra Daruich; Couanon Marie; Matthieu P Robert; Dominique Bremond-Gignac
Journal:  Drugs       Date:  2022-09-08       Impact factor: 11.431

Review 3.  Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature.

Authors:  Maria Sofia Falzarano; Alessandra Ferlini
Journal:  J Clin Med       Date:  2019-05-08       Impact factor: 4.241

Review 4.  Dental-craniofacial manifestation and treatment of rare diseases.

Authors:  En Luo; Hanghang Liu; Qiucheng Zhao; Bing Shi; Qianming Chen
Journal:  Int J Oral Sci       Date:  2019-02-20       Impact factor: 6.344

5.  Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa.

Authors:  C Has; L Liu; M C Bolling; A V Charlesworth; M El Hachem; M J Escámez; I Fuentes; S Büchel; R Hiremagalore; G Pohla-Gubo; P C van den Akker; K Wertheim-Tysarowska; G Zambruno
Journal:  Br J Dermatol       Date:  2019-08-09       Impact factor: 9.302

6.  A de novo mutation in KRT5 in a crossbred calf with epidermolysis bullosa simplex.

Authors:  Joana G P Jacinto; Irene M Häfliger; Inês M B Veiga; Cord Drögemüller; Jørgen S Agerholm
Journal:  J Vet Intern Med       Date:  2020-11-02       Impact factor: 3.333

7.  Kidney and Urinary Tract Involvement in Epidermolysis Bullosa: Is Routine Follow-Up Necessary?

Authors:  Neslihan Cicek; Nurdan Yildiz; Ruslan Asadov; Ayse Deniz Yucelten; Halil Tugtepe; Harika Alpay
Journal:  Dermatol Pract Concept       Date:  2021-05-20

8.  Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases.

Authors:  Yueqian Yu; Zhenzhen Wang; Zihao Mi; Lele Sun; Xi'an Fu; Gongqi Yu; Zheng Pang; Hong Liu; Furen Zhang
Journal:  Acta Derm Venereol       Date:  2021-07-15       Impact factor: 3.875

9.  Profiling trial burden and patients' attitudes to improve clinical research in epidermolysis bullosa.

Authors:  Christine Prodinger; Anja Diem; Katherina Ude-Schoder; Josefina Piñón-Hofbauer; Sophie Kitzmueller; Johann W Bauer; Martin Laimer
Journal:  Orphanet J Rare Dis       Date:  2020-07-10       Impact factor: 4.123

10.  Novel biallelic variants in COL7A1 cause recessive dystrophic epidermolysis bullosa.

Authors:  Neng Yang; Yongyi Ma; Hong Yao; Qing Chang; Victor Zhang; Zhiqing Liang; Xiongwei Cai
Journal:  Mol Genet Genomic Med       Date:  2020-06-14       Impact factor: 2.183

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