Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome
This is a multicenter genetic study aimed at identifying new genes/variants associated with sudden infant death syndrome (SIDS) based on whole-genome sequencing of family trios
• Death of a child between 0 and 2 years of age due to sudden unexpected death in infant
• Child included in the French SUDI registry with effective participation in the biocollection
• Children who also meet the inclusion criteria for the BIOMINRISK-NEUROBIO (axis 2) and BIOMINRISK-RADIO-ANAT (axis 3) studies in the overall BIOMINRISK project.
• Biological parents of the child included in the BIOMINRISK study
• Parents who have both signed the consent form for blood collection and inclusion of their samples in the biocollection
• parents beneficiaries of a social security or similar scheme