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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

Updates are delayed or unverified. Check original sources for the latest information.

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ICD Q79.6ORPHA:98249EDS

Ehlers-Danlos Syndrome

Ehlers-Danlos syndrome is a group of genetic conditions affecting connective tissue. It causes joints to be unusually flexible and skin to be more stretchy or fragile. Symptoms vary widely. There is no cure, but treatments help manage pain and prevent injury.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

816
Articles
45
Trials
Data refreshed
19 October 2026
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Common Questions

What is Ehlers-Danlos Syndrome?

Ehlers-Danlos syndrome is a group of genetic conditions affecting connective tissue. It causes joints to be unusually flexible and skin to be more stretchy or fragile. Symptoms vary widely. There is no cure, but treatments help manage pain and prevent injury.

How many clinical trials are available for Ehlers-Danlos Syndrome?

RareWays currently indexes 45 clinical trials for Ehlers-Danlos Syndrome, of which 6 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Ehlers-Danlos Syndrome come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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