Rare disease study aims to unlock mysteries of peroxisome disorders
NCT ID NCT01668186
First seen Jan 07, 2026 · Last updated May 23, 2026 · Updated 15 times
Summary
This study follows 244 people with peroxisome biogenesis disorders (PBD), a group of rare inherited conditions that affect development and metabolism. Researchers will collect medical records, blood, urine, and imaging data over 5 years to better understand the disease and improve care. Participants can join from anywhere, even if they cannot visit the clinic.
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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.
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.
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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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