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GALAXY is a registry research study that plans to learn more about individuals with X&Y variations (also called sex chromosome aneuploidies) through collecting information from medical records.This includes genetic tests, imaging, medications, and more for hundreds of patients seen at a number of clinics across the US. The purpose of the GALAXY Registry is to collect and store this information with the overall goal to improve health outcomes in individuals with X&Y variations and the care they receive.
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Exclusion criteria
a. Lack of documentation of genetic testing confirming SCA diagnosis
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Central trial contact
Shanlee M Davis, MD, PhD
Data sourced from clinicaltrials.gov
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