Screening study for CLN2 disease in 6-year-olds
Treatments studied
Part of Brain & nervous system, Genetic & congenital clinical trials.
This study is screening children for a rare genetic condition called CLN2 disease. It looks for signs like seizures, speech loss, and movement problems to find out how common this condition is among 6-year-olds.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child must be exactly 6 years old.
- Your child must have had at least one seizure that started for no clear reason.
- Your child must have a problem with speech or movement, or show certain brain changes on an EEG or MRI.
- The seizures and problems cannot be due to birth injury, head trauma, or a brain defect.
- Your child must not have been diagnosed with CLN2 disease before.
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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