ICD Q81ORPHA:79361EB

Epidermolysis Bullosa

Epidermolysis bullosa is a group of rare genetic conditions that cause extremely fragile skin that blisters and tears easily. It affects the proteins that anchor skin layers together. Severity ranges from mild to life-threatening. Gene therapy and advanced wound care are transforming treatment.

696
Articles
103
Trials (4 AU)
Updated
25 March 2026
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Common Questions

What is Epidermolysis Bullosa?

Epidermolysis bullosa is a group of rare genetic conditions that cause extremely fragile skin that blisters and tears easily. It affects the proteins that anchor skin layers together. Severity ranges from mild to life-threatening. Gene therapy and advanced wound care are transforming treatment.

How many clinical trials are available for Epidermolysis Bullosa?

RareWays currently indexes 103 clinical trials for Epidermolysis Bullosa, of which 22 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Epidermolysis Bullosa come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.