Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Scientists seek genetic clues behind rare adrenal disease and tumor syndromes

NCT ID NCT00001452

First seen Oct 31, 2025 · Last updated May 23, 2026 · Updated 35 times

Summary

This study looked at people with rare conditions that cause hormone problems and tumors, like PPNAD and Carney Complex. Researchers aimed to find the genetic causes and link them to specific symptoms. Over 1,300 participants, including patients and their family members, were involved to improve diagnosis and genetic counseling.

Disclaimer Read more

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for CUSHING'S SYNDROME are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

Conditions

Explore the condition pages connected to this study.