Purpan University Hospital
Toulouse, 31059, France
Location status: Recruiting
NCT Number: NCT05202210
The present study will establish a collection of biological samples from Noonan patients to be used for research purposes only, with due respect for confidentiality.
Interested in participating?
Request Info18 year–99 year
All sexes
Observational
Toulouse, 31059, France
Location status: Recruiting
Noonan syndrome is a rare autosomal dominant genetic disorder characterized by a combination of typical facial features, heart defects, short stature, skeletal abnormalities, mild developmental delay and a predisposition to myeloproliferative disorders. This syndrome is caused by germline mutations in genes encoding components or regulators of the Rat Sarcoma (RAS) / extracellular signal-regulated kinase (ERK) signaling pathway, which is essential for cell cycle differentiation, growth, and senescence.
Patients with Noonan syndrome or related diseases are followed at the children's hospital, Toulouse University Hospital. During regular check-up visits, an extra sample of blood and urine will be collected and stored for research utilisation with the patient's consent. The ultimate objective of this collection is to provide available biological resources to facilitate the development of subsequent studies aimed at better characterizing the multisystemic disorders in Noonan syndrome, to understand the pathophysiology of the disease, and to identify biological factors that predict the severity and progression of the disease. The possibility of having systematically collected biological resources will make it possible to answer certain questions more quickly depending on the progress of research.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
extra sample of blood and urine will be collected
Time frame: inclusion
extra sample of blood and urine will be collected
Contact information is provided by the study sponsor or research team.
Françoise Auriol, PhD
CONTACT
5 67 77 10 95 ext. 0033
Thomas EDOUARD, MD, PhD
CONTACT
5 34 55 85 55 ext. 0033
University Hospital, Toulouse
Other
Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome and to Identify Predictive Factors of Disease Progression
Acronym: Noonan
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04888936
Abnormalities, Multiple, Capillary Arteriovenous Malformation Syndrome
Bethesda, Maryland, United States
View Trial DetailsNCT06668805
Bone Diseases, Bone Diseases, Developmental
Los Angeles, California, United States
View Trial DetailsNCT07464821
Cardiovascular Abnormalities, Cardiovascular Diseases
Alessandria, Italy
View Trial DetailsNCT05361811
Abnormalities, Multiple, Cardiofaciocutaneous Syndrome
Bethesda, Maryland, United States
View Trial Details