Study genetics in identical twin who differ in symptoms
Part of Genetic & congenital clinical trials.
This study looks at DNA changes to explain why two identical (monozygotic) twins can have different symptoms. It may help clarify the cause of an unclear condition in one twin so the right diagnosis (and future treatment) can be found.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are part of a pair of identical (same DNA) twins
- The twins have different observable symptoms or findings (one twin is affected differently)
- Your doctors do not yet have a clear diagnosis
- A genetic (DNA-related) cause is suspected for the condition in one twin
- Both twins (or their legal representatives) must agree to join the study
- There must be a clear difference in the twins’ symptoms or exam findings
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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