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11 sty 2024 · Epidermolysis bullosa (EB) defines a prototypic group of rare, inherited dermatoses, characteristically featuring skin fragility secondary to structural defects in the dermo-epidermal junction. This skin fragility creates an impaired tolerance to mechanical stress.
This cross-sectional and longitudinal study determines the incidence and prevalence of epidermolysis bullosa stratified by subtype in the United States
1 maj 2022 · Prevalence rates were calculated per million population [total number of patients with EB alive at a specific timepoint (22 April 2021)/total population × 1 000 000]. Statistical analyses were conducted using GraphPad Prism version 9·1·2 (GraphPad Software, San Diego, CA, USA).
Objectives: To quantify prevalence, incidence and mortality of EB in England and Wales. Methods: Demographic data for patients in England and Wales were collected on a secure electronic database, prospectively from January 2002 to April 2021 and retrospectively for cases prior to 2002.
Providing a precise diagnosis is the first step in approaching a patient suspected with EB and will yield invaluable prognostic information. The diagnosis of EB is based on a combination of clinical features, family history and laboratory findings.
24 wrz 2020 · Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses characterized by mucocutaneous fragility and blister formation, inducible by often minimal trauma.
Epidermolysis bullosa: a 2020 perspective Br J Dermatol. 2020 Oct;183(4):603. doi: 10.1111/bjd.19125. Epub 2020 May 10. Author E Pope 1 2 Affiliations 1 The ... Epidermolysis Bullosa* / epidemiology Humans Skin Abnormalities* ...
