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Prader-Willi Syndrome (PWS) is a rare syndrome with a prevalence of 15 to 20 000 at birth. PWS represents a large fraction of mental retardation syndromes due to a genetic cause and the most frequent ...
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Lead Sponsor
University Hospital, Toulouse
NCT06573723 · Rare Diseases, Amyloidosis, and more
NCT04463316 · Prader-Willi Syndrome, PWS-like Syndrome, and more
NCT06420297 · Hyperphagia in Prader-Willi Syndrome
NCT05701774 · Prader-Willi Syndrome
NCT02263781 · Hypotonia-Cystinuria Syndrome, Muscle Hypotonia, and more
University Hospital of Children
Toulouse
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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