Scientists hunt for genes behind rare kidney condition
NCT ID NCT00925379
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how often kidney hypodysplasia (a condition where one or both kidneys are small and underdeveloped) runs in families. Researchers collected DNA from 342 children aged 3 months to 18 years to try to find genes that may cause the condition. The goal was to better understand its genetic basis, not to test a treatment.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this study could help identify genes linked to kidney hypodysplasia, paving the way for future genetic testing or understanding of the condition.
- What could go wrong
- This is an observational study, not a treatment trial. It may not find clear genetic links, and any findings would need much more research before they could help patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Necker Hospital
Paris, 75015, France