Condition
Epidermolysis Bullosa Simplex
Dermatology
Overview
A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Epidermolysis Bullosa Simplex
- Topic type
- Condition
- Category
- Dermatology
- MeSH classification
- C16.131.831.493.180|C16.320.850.275.180|C17.800.804.493.180|C17.800.827.275.180|C17.800.865.410.180
Preparing for an appointment about Epidermolysis Bullosa Simplex
If you are speaking with a healthcare professional about Epidermolysis Bullosa Simplex, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.