Scientists track rare genetic disorders to unlock better care
NCT ID NCT01668186
Summary
This study aims to better understand a group of rare, inherited disorders called peroxisome biogenesis disorders (PBDs). Researchers will follow about 244 patients over time, collecting health records, images, and samples to map out how these diseases progress. The goal is to identify patterns, improve management guidelines, and find potential targets for future treatments.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Research Institute of the McGill University Health Center
RECRUITINGMontreal, Quebec, H4A 3J1, Canada
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Conditions
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