Research network for hereditary spastic paraplegia
Part of Brain & nervous system, Genetic & congenital clinical trials.
This trial aims to build a research network and gather information from people with two genetic types of hereditary spastic paraplegia (SPG4 and SPG5A). It will help doctors better understand these conditions and improve care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a genetic diagnosis of either SPG4 or SPG5A (these are specific types of hereditary spastic paraplegia).
- You can be any age—children and adults are welcome.
- You must have both a clinical and a genetic diagnosis.
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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