Clin2
NCT06274164Possibly a fitRecruiting

RAI1 gene disorder study: biomarkers and clinical features

RAI1 Gene 17P11.2 Deletion+Duplication

Treatments studied

Part of Brain & nervous system, Genetic & congenital clinical trials.

This study looks at people with a rare genetic condition caused by changes in the RAI1 gene. Researchers want to learn more about the condition and find markers that could help with future treatments. You and a healthy family member will spend one day in Houston for tests and samples.

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

Phase
N/A
Enrollment
90 people
Ages
1 month to 80 years
Study type
Observational

Who can take part

  • You or your child must have a confirmed diagnosis of an RAI1-related disorder through genetic testing.
  • Must be between 1 month and 60 years old.
  • Must have good hearing and vision (based on parent report).
  • Must be able to travel to Houston, Texas, and spend one full day there.
  • The caregiver must speak and understand English to give permission.
  • You cannot be in another treatment study at the same time.

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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