Genetic Cancer Risk Screening Survey
Part of Blood & lymphatic, Bones, joints & muscles, Cancer, Genetic & congenital, Hormones & metabolism, Skin clinical trials.
This study screens people who may have an inherited risk for certain cancers due to their personal or family medical history or known gene changes. By completing a survey, you can help researchers find the right study for you and learn more about your cancer risk.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You or a close family member has had a rare type of cancer, multiple cancers, or cancer at an unusually young age (like before age 45).
- You or a family member may have an inherited cancer syndrome, such as Li-Fraumeni, Fanconi anemia, or a RASopathy.
- You have a known gene change (like TP53, DICER1) that increases cancer risk, or you may be a carrier of one.
- You or a family member has a condition that affects the bone marrow, like Diamond-Blackfan anemia or severe congenital neutropenia.
- You are willing to complete a survey about your medical and family history to see if you qualify for a specific study.
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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