Silver Russell syndrome and parent fertility study
Part of Bones, joints & muscles, Genetic & congenital clinical trials.
This study looks at how parent fertility and assisted reproductive technology might be linked to Silver Russell syndrome. It aims to understand the condition better by asking parents of affected patients about their experiences.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must be 18 years old or older.
- You must be the parent of a patient with Silver Russell syndrome who is being followed at the Pediatric Endocrinology department of the hospital.
- You must not object to participating in the study.
- You must not be receiving state medical aid.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study looks at how young adults aged 15–25 with rare genetic conditions (like certain bone, skin, hearing, or facial conditions) are doing in school, work, and social life. Researchers want to understand what helps or prevents young people with these conditions from being included in their communities.
This study looks at fertility in women with polycystic ovary syndrome (PCOS) compared to women without it, to better understand how PCOS affects fertility. If you have PCOS or have normal hormones and metabolism, and you were part of a previous study called METABOPK, you may be able to join.
This study measures how much copper is present in breast milk in people with Wilson’s disease. It aims to provide safer guidance for breastfeeding during treatment, including during pregnancy.
This study is for people who have a rare syndrome or rare congenital condition and are seen at a rare-disease clinic. It aims to better understand these conditions and how care works in a team setting, which may help guide future treatment decisions.
This study looks at mental health symptoms in people with White-Sutton syndrome, a rare genetic condition. By answering questions, you can help doctors better understand what challenges people face and how to support them.
This study looks at rare genetic syndromes caused by changes in the RNU4ATAC or RTTN genes. It aims to understand how these changes affect the body by studying patients, their parents, and fetal tissue.
Hear when a new Syndrome, Russell Silver trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.