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Turner Syndrome: Genetic Considerations

Recruitingn/aAges 1 Day - 110 YearsAllEunice Kennedy Shriver National Institute of Chil…
NCT07502586 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Background: Turner syndrome (TS) is a rare genetic condition. It happens when a person is born missing all or part of an X sex chromosome. People with TS can have heart defects, short stature, autoimmune conditions, and malformations. Many women with TS never have periods and cannot conceive; however, some women have normal ovaries (egg cells). Researchers want to learn more about why some women with TS are fertile and others are not. To do this, they need to be able to compare the genes of many women who have TS. Objective: To create a genetic database of people with TS. Eligibility: People of any age with TS currently enrolled, or interested in enrolling in protocol 20-CH-0126. Biological parents and other relatives are also needed. Design: Participants who agree to join this study will be asked to enroll in a second study; that study is called "NIAID Centralized Sequencing Prot

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📋 Eligibility rules (as published)
* INCLUSION CRITERIA: 1. Turner syndrome diagnosis based on karyotype 2. Any age 3. Biological parent of Turner syndrome patient 4. Relatives of Turner syndrome patient 5. The subject from protocol 20CH0126 will enroll in this study only when they agree to be referred to the 17I0122 NIAID study. They can withdraw participation in the 17I0122 study if they do not want to have their genetic data in this database EXCLUSION CRITERIA: 1\. Diagnosis other than Turner syndrome
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What it tests

  • Not listed
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Where

1 site
National Institutes of Health Clinical Center
Bethesda, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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