Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
Background Several new genes and clinical subtypes have been identified since the
publication in 2014 of the report of the last International Consensus Meeting on …
publication in 2014 of the report of the last International Consensus Meeting on …
[HTML][HTML] Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa
M El Hachem, G Zambruno, E Bourdon-Lanoy… - Orphanet Journal of …, 2014 - Springer
Background Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group
of rare diseases characterized by fragility and blistering of skin and mucous membranes …
of rare diseases characterized by fragility and blistering of skin and mucous membranes …
Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?
R Baardman, VK Yenamandra… - Journal of the …, 2021 - Wiley Online Library
Background Epidermolysis bullosa (EB) is a heterogeneous group of rare and incurable
genetic disorders characterized by fragility of the skin and mucosae, resulting in blisters and …
genetic disorders characterized by fragility of the skin and mucosae, resulting in blisters and …
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
JD Fine, RAJ Eady, EA Bauer, JW Bauer… - Journal of the American …, 2008 - Elsevier
BACKGROUND: Since publication in 2000 of the Second International Consensus Report
on Diagnosis and Classification of Epidermolysis Bullosa, many advances have been made …
on Diagnosis and Classification of Epidermolysis Bullosa, many advances have been made …
Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification
JD Fine, L Bruckner-Tuderman, RAJ Eady… - Journal of the American …, 2014 - Elsevier
Background Several new targeted genes and clinical subtypes have been identified since
publication in 2008 of the report of the last international consensus meeting on diagnosis …
publication in 2008 of the report of the last international consensus meeting on diagnosis …
Inherited epidermolysis bullosa: new diagnostics and new clinical phenotypes
Inherited epidermolysis bullosa (EB) is a group of heterogeneous genetic disorders
characterized by skin fragility. EB comprises a large spectrum of phenotypes, ranging from …
characterized by skin fragility. EB comprises a large spectrum of phenotypes, ranging from …
Inherited epidermolysis bullosa: new diagnostic criteria and classification
LRA Intong, DF Murrell - Clinics in dermatology, 2012 - Elsevier
Epidermolysis bullosa (EB) is a group of inherited, mechanobullous disorders caused by
mutations in various structural proteins in the skin. There have been several advances in the …
mutations in various structural proteins in the skin. There have been several advances in the …
[HTML][HTML] Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases
H Montaudié, C Chiaverini, E Sbidian… - Orphanet journal of rare …, 2016 - Springer
Background Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group
of rare diseases characterized by exacerbated skin and/or mucosal fragility and blister …
of rare diseases characterized by exacerbated skin and/or mucosal fragility and blister …
[HTML][HTML] Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa
C Has, L Liu, MC Bolling, AV Charlesworth… - The British Journal of …, 2020 - ncbi.nlm.nih.gov
The overall objective of this guideline is to provide the user with information on the
laboratory diagnosis of inherited epidermolysis bullosa (EB) to improve outcomes (Table 1) …
laboratory diagnosis of inherited epidermolysis bullosa (EB) to improve outcomes (Table 1) …
The clinical spectrum of epidermolysis bullosa simplex
HM Horn, MJ Tidman - British Journal of Dermatology, 2000 - academic.oup.com
As part of the UK National Epidermolysis Bullosa Register, we have systematically recorded
clinical information on 130 (77%) of the 168 known Scottish epidermolysis bullosa simplex …
clinical information on 130 (77%) of the 168 known Scottish epidermolysis bullosa simplex …