Clinical and Genetic Aspects in Fetuses and Children With Sex Chromosome Disorders
Enrolling by invitation
Conditions studied: Sex Chromosome Disorders
In brief
The aim of the project is to: 1. Investigate organ development and growth in fetuses with sex chromosome disorders; 2. Investigate growth, development, and morbidity in children with sex chromosome disorders during the first years of life; 3. Delineate how variations in sex chromosome number affect the epigenetic and genetic mechanisms regulating gene expression in the placenta and in multiple tissues of the child after birth over time during early childhood; 4. Investigate the gut microbiome in children with sex chromosome disorders during the first years of life; 5. Identify the epigenetic and genetic mechanisms and placental and child-specific alterations underlying the phenotype observed in fetuses, children, and adults with sex chromosome disorders, using a deep phenotyping approach.
Key facts
- Study ID
- NCT07341412
- Run by
- University of Aarhus
- People needed
- 300
- Starts
- 2024-09-01
- Expected to finish
- 2034-01-01
- Last updated by the study team
- 2026-01-14
Who can join
Age: any, up to 50. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Aarhus University Hospital — Aarhus, Denmark
Full record on ClinicalTrials.gov
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