Scientists uncover genetic secrets behind rare hormone disorders
NCT ID NCT00001452
First seen Oct 31, 2025 · Last updated May 16, 2026 · Updated 33 times
Summary
This study looked at the genes and health patterns of people with rare conditions like PPNAD, Carney Complex, and Peutz-Jeghers syndrome. Researchers studied over 1,300 participants to find the genetic causes and improve diagnosis. The goal was to help families understand their risk and guide future care.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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