Biobank study for people with Noonan syndrome
Part of Bones, joints & muscles, Genetic & congenital, Heart & circulation, Skin clinical trials.
This study collects biological samples to better understand what causes Noonan syndrome. If you qualify, your participation could help researchers learn how the condition works and guide future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have Noonan syndrome (child age 3+ or adult)
- You are covered by the French social security system (or benefit from it)
- You can read and understand the study information in French
- You (or your legal representative) agree to participate and do not object
- You are not pregnant and not breastfeeding
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 whether people with Noonan syndrome have unusual bleeding or blood clotting problems. It aims to better understand these issues so doctors can offer better care.
This study looks at cholesterol and fat levels in people with Noonan syndrome or related conditions. It aims to understand how these levels change with age, gender, and genetic cause.
This trial is a real-world registry that collects information about children with Noonan syndrome who are treated with Norditropin (a growth hormone). It helps researchers understand how these children do over time in routine care.
This study collects and stores health samples and information from people with RASopathy conditions (like Noonan or Costello syndromes) and from family members who may not have the condition. It helps researchers understand these disorders and supports future studies that could lead to better care.
This trial tests a new drug, vosoritide, to help children with Noonan syndrome who are still growing but are shorter than expected despite growth hormone treatment. It aims to see if the drug can improve their growth.
This study collects biological samples and related health information for people with Marfan syndrome or similar inherited conditions. It helps researchers better understand these conditions and may lead to improved care for patients in the future.
Hear when a new Noonan Syndrome trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.