Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The clinical spectrum of epidermolysis bullosa simplex.

The British journal of dermatology - 1 Mar 2000

Horn H M, Tidman M J

Abstract excerpt

As part of the U.K. National Epidermolysis Bullosa Register, we have systematically recorded clinical information on 130 (77%) of the 168 known Scottish epidermolysis bullosa simplex (EBS) sufferers. Three subtypes of EBS were recognized: Dowling-Meara (EBS-DM), Weber-Cockayne (EBS-WC) and Köbner (EBS-Kb), seen in 5%, 42% and 53% of patients, respectively. As there is considerable overlap between EBS-WC and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Infant, Newborn
Share to Mouth Mucosa
Share to Pedigree

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Age of Onset

Share to Disease Progression

Share to Epidermolysis Bullosa Simplex

Share to Infant

Source

Identifiers

PMID: 10735952
DOI: 10.1046/j.1365-2133.2000.03358.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The clinical spectrum of epidermolysis bullosa simplex.PMID 10735952Read ↗

The clinical spectrum of dystrophic epidermolysis bullosa.Semantic proximity Read ↗

Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.Semantic proximity Read ↗

Recently Identified Forms of Epidermolysis BullosaSemantic proximity Read ↗

Inherited epidermolysis bullosa: update on the clinical and genetic aspectsSemantic proximity Read ↗

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.Semantic proximity Read ↗

Inherited epidermolysis bullosaSemantic proximity Read ↗

Hereditary epidermolysis bullosa.Semantic proximity Read ↗

Genetic Profile of Epidermolysis Bullosa Cases in King Abdulaziz Medical City, Riyadh, Saudi ArabiaSemantic proximity Read ↗

Pain in recessive dystrophic epidermolysis bullosa (RDEB): findings of the Prospective Epidermolysis Bullosa Longitudinal Evaluation Study (PEBLES)Semantic proximity Read ↗

Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa.Semantic proximity Read ↗

Epidermolysis Bullosa. Clinical, Epidemiologic, and Laboratory Advances and the Findings of the National Epidermolysis Bullosa RegistrySemantic proximity Read ↗

Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic versus Non-Syndromic Skin Fragility DisordersSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.