ICD J98.09ORPHA:244PCD

Primary Ciliary Dyskinesia

Primary ciliary dyskinesia is a rare genetic condition caused by defective cilia function, leading to chronic respiratory infections, bronchiectasis, and fertility problems. Kartagener syndrome (with situs inversus) is a subset. It is significantly underdiagnosed. No disease-modifying therapies currently exist, but several are in trials.

517
Articles
70
Trials (1 AU)
Updated
26 March 2026
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Common Questions

What is Primary Ciliary Dyskinesia?

Primary ciliary dyskinesia is a rare genetic condition caused by defective cilia function, leading to chronic respiratory infections, bronchiectasis, and fertility problems. Kartagener syndrome (with situs inversus) is a subset. It is significantly underdiagnosed. No disease-modifying therapies currently exist, but several are in trials.

How many clinical trials are available for Primary Ciliary Dyskinesia?

RareWays currently indexes 70 clinical trials for Primary Ciliary Dyskinesia, of which 21 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Primary Ciliary Dyskinesia 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.