A network for rare brain vessel diseases
Part of Brain & nervous system, Genetic & congenital, Heart & circulation, Hormones & metabolism, Skin clinical trials.
This study creates a large Italian network to help diagnose and understand rare cerebrovascular diseases like CADASIL, Fabry's disease, and Moyamoya. It aims to improve care for people with these conditions.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a diagnosis of a rare cerebrovascular disease, such as CADASIL, Fabry's disease, COL4A1, Sneddon's syndrome, or Moyamoya.
- The diagnosis is based on clinical signs, genetic testing, or brain imaging results.
- You have had at least one brain MRI scan.
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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