Clin2
NCT04395495Possibly a fitRecruiting

RASopathy disorder study biobank for kids and families

RAS MutationNeurofibromatosis 1Noonan SyndromeNoonan Syndrome With Multiple LentiginesNoonan Neurofibromatosis SyndromeCardiofaciocutaneous SyndromeCostello SyndromeLegius Syndrome

Part of Bones, joints & muscles, Brain & nervous system, Cancer, Genetic & congenital, Heart & circulation, Skin clinical trials.

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.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You (or the person) have a suspected or confirmed RASopathy (such as Noonan, Costello, or neurofibromatosis types)
  • Or you are an unaffected relative of someone with a suspected or confirmed RASopathy
  • The diagnosis is okay if it’s based on a clinician’s assessment and/or genetic testing
  • The person can take part in the study’s informed consent process (with parent/guardian consent if needed)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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