Studies of the Variable Phenotypic Presentations of Rapid-Onset Dystonia Parkinsonism and Other Movement Disorders

Launched by STATE UNIVERSITY OF NEW YORK AT BUFFALO · May 21, 2008

Keywords

ClinConnect Summary

This clinical trial is focused on understanding a rare condition called rapid-onset dystonia-parkinsonism (RDP), which affects a person's movement and muscle control. The study aims to find individuals who either have RDP or carry specific genetic changes related to the condition. Researchers want to learn more about how common RDP is and how it develops over time in those affected.

If you or someone you know has symptoms that match RDP or has been diagnosed with this condition, you may be eligible to participate in the trial. The study is open to people of all ages and genders, and they are currently looking for participants. There are no specific exclusions, meaning that if you meet the criteria, you can join. As a participant, you can expect to provide information about your health and possibly undergo tests to help researchers gather important data about this condition. Your involvement could help improve understanding and treatment options for RDP in the future.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • clinical presentation consistent with ATP1A3 disease (RDP, AHC) or confirmed diagnosis of RDP or AHC
• Exclusion Criteria:
• • none