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Epidermolysis Bullosa (EB)
Epidermolysis bullosa (EB), is a rare, heterogenous group of inherited skindisorders that causes extreme skin fragility, leading to painful blistering withminimal mechanical friction or trauma. EB can affect not only the skin but also mucous membranes, the epithelial-lined tissue and internal organs, significantly impacting quality of life. There are currently no curative treatments for any of the four major classic
types of EB or their subtypes. Accurate diagnosis and timely referral are crucial for effective symptom management and long-term care. EB shares clinical features with a range of other conditions — from immunobullous disorders to more common infections such as impetigo or tinea — making differentiation in primary care both essential and challenging.
Resource details
| Contributed by: | Information and support available for patients with the genetic skin blistering conditions known as epidermolysis bullosa (EB) |
| Authored by: |
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| Licence: | © All rights reserved More information on licences |
| First contributed: | 09 December 2025 |
| Audience access level: | General user |
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