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

Gå till den engelska sidan

Scientists track gene mutation behind two brain diseases

NCT ID NCT01925196

First seen Nov 01, 2025 · Last updated May 25, 2026 · Updated 29 times

Summary

This study followed 50 adults with a specific gene mutation (C9ORF72) that can cause either ALS or frontotemporal dementia. Researchers tracked changes in strength, thinking, memory, and behavior over three years using brain scans, spinal fluid tests, and other exams. The goal was to understand how the same gene leads to different diseases and to find biomarkers that could help detect or measure disease progression in the future.

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 AMYOTROPHIC LATERAL SCLEROSIS 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.