Clin2
NCT03492060Possibly a fitRecruiting

Study of genetic variants in neurogenetic disorders over time

Neurodevelopmental DisordersIntellectual DisabilityDevelopmental DelayAutism Spectrum DisorderSeizuresHypertonia, MuscleHypotonia

Part of Brain & nervous system, Mental health clinical trials.

This study looks at how people’s genetic test results relate to health changes over time in conditions caused by gene differences. If you already have genetic confirmation of a disease-causing variant, you may be able to join.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You must have had whole genome or whole exome genetic testing done
  • You must have a confirmed genetic variant found in any gene
  • Your genetic test must clearly show a harmful (disease-causing) variant
  • You must be able to provide proof of your genetic results
  • If you don’t have confirmed genetic results, you may not be eligible

View the official record on ClinicalTrials.gov

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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