Scientists map brain connections in rare movement disorders

NCT ID NCT03481491

Summary

This study aimed to understand how two key brain areas—the basal ganglia and cerebellum—interact in people with specific genetic forms of dystonia, a movement disorder. Researchers compared brain scans from 104 participants, including patients with ADCY5 or PRRT2 gene mutations and healthy volunteers. They used functional MRI and mild, non-invasive brain stimulation to see if stimulating the cerebellum changes activity in other motor control networks.

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 DYSTONIA are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • Département de Neurologie, Fédération des Maladies du Système Nerveux, GH Pitié-Salpêtrière, 47 Bd de l'Hôpital

    Paris, France

Conditions

Explore the condition pages connected to this study.