Study of sex chromosome disorders in fetuses and children
Part of Genetic & congenital, Heart & circulation, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.
This study looks at the genetic and physical health of babies and children who have a sex chromosome disorder (like having an extra or missing X or Y chromosome). It also compares them to children without these conditions. The goal is to learn more about how these disorders affect development.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You or your baby must be at least 18 years old if you are a mother or pregnant person joining the study
- Your baby or child must have a confirmed sex chromosome disorder (like XXY, XYY, or Turner syndrome) for the case group
- You must be willing to give written permission (informed consent) to join the study
- If your child is in the study and you share custody, both parents must give permission
- You or your child cannot have severe claustrophobia or any implanted metal that would make an MRI unsafe
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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