The purpose of this study is to explore familial cancer. It investigates genetic factors that may contribute to cancer development in families with a history of the condition.
The study focuses on identifying genetic variants that could be linked to familial cancer. It evaluates these variants to enhance understanding and potentially improve diagnosis and care for hereditary cancer.
- Who can participate: Individuals with a history of cancer diagnosed under 26 years of age and relatives with early-onset cancer may participate. Those with multiple cancers or rare pediatric cancers, and their family members, are also eligible.
- Study details: Participants will provide blood, saliva, or skin samples for genetic analysis. These samples are stored for study purposes, and leftover tumor samples may also be analyzed. A placebo is not involved in this study.