New study seeks clues to rare brain disorder

NCT ID NCT01425944

First seen Mar 02, 2026 · Last updated May 15, 2026 · Updated 10 times

Summary

This study aims to learn more about Sturge-Weber syndrome, a rare condition that affects the brain and skin. Researchers will study 600 participants to find links between genetic changes, blood vessel patterns, and disease severity. The goal is to improve how doctors monitor and care for people with this condition.

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 STURGE-WEBER SYNDROME are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • Baylor College of Medicine/Texas Children's Hospital

    Houston, Texas, 77030, United States

  • Cincinnati Children's Hospital

    Cincinnati, Ohio, 45229, United States

  • Kennedy Krieger Institute

    Baltimore, Maryland, 21205, United States

  • Nationwide Children's Hospital

    Columbus, Ohio, 43205, United States

  • New York University

    New York, New York, 10016, United States

  • Wayne State University/Children's Hospital of Michigan

    Detroit, Michigan, 48201, United States

  • Wills Eye Institute

    Philadelphia, Pennsylvania, 19107, United States

Conditions

Explore the condition pages connected to this study.