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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.

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ICD I67.5ORPHA:2573

Moyamoya Disease

Moyamoya disease is a rare condition in which the large arteries at the base of the brain slowly narrow, and a network of small, fragile vessels forms to compensate. It can cause strokes, mini-strokes and seizures in children and adults. Treatment includes surgery to improve blood flow to the brain and medicines to lower stroke risk.

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

767
Articles
32
Trials
Data refreshed
19 October 2026
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Common Questions

What is Moyamoya Disease?

Moyamoya disease is a rare condition in which the large arteries at the base of the brain slowly narrow, and a network of small, fragile vessels forms to compensate. It can cause strokes, mini-strokes and seizures in children and adults. Treatment includes surgery to improve blood flow to the brain and medicines to lower stroke risk.

How many clinical trials are available for Moyamoya Disease?

RareWays currently indexes 32 clinical trials for Moyamoya Disease, of which 7 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 Moyamoya Disease 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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