Brain smell pathways in Prader-Willi syndrome
Part of Brain & nervous system, Genetic & congenital, Hormones & metabolism clinical trials.
This study uses MRI scans and smell tests to understand how the brain processes smells in children with Prader-Willi syndrome. It may help explain why some children have trouble with smell and could lead to better care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child has a confirmed genetic diagnosis of Prader-Willi syndrome
- The genetic subtype (deletion or non-deletion) is known
- Your child is between 5 and 7 years old
- Your child has a planned hospital stay at the Toulouse reference center for PWS
- Your child does not have any metal implants or other reasons that would make an MRI unsafe
- Your child is not allergic to any of the fragrances used in the smell test
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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