DNA hunt for hidden genes in common birth defect
NCT ID NCT02495090
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 60 people with a family history of hypospadias, a birth defect where the opening of the penis is not at the tip. Researchers used DNA sequencing to find new genetic changes linked to the condition. The goal was to discover genes that may cause hypospadias when passed down in families.
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 could help identify new genes involved in hypospadias, potentially leading to better genetic counseling or future treatments.
- What could go wrong
- This is a small, completed genetic study with no direct treatment. It only looks for gene variants, so it may not lead to any new therapies.
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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
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Locations
-
Hôpital Lapeyronie
Montpellier, 34295, France
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