French Cohort on Neonatal Cerebral Artery Infarction FRESH-PEF60090-en Stéphane CHABRIER French Cohort on Neonatal Cerebral Artery Infarction AVCNN FRESH-PEF60090-en 60090 FRESH-PEF60090 Stéphane CHABRIER CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT-ETIENNE Epidemiology France Portal (PEF) APF FRANCE HANDICAP (APF) CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT-ETIENNE FONDATION GARCHES INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) MINISTERE DU TRAVAIL, DE LA SANTE, DES SOLIDARITES ET DES FAMILLES null Stéphane;CHABRIER History miscarriage primiparity first gestation twin pregnancy premature rupture of membranes caesarean section foetal distress monitoring medical care reeducation and rehabilitation information Physical and Rehabilitation Medicine Paediatrics Biological determinants: Genetic predisposition Biological determinants General objective: to determine the clinical and biological obstetric-neonatal profile for full-term newborns presenting symptomatic arterial ischaemic stroke. Secondary objectives: - to determine the mechanisms of infarction from obstetric history, laboratory tests and imaging. - To monitor motor, cognitive and epileptic outcomes in children as well as their autonomy and quality of life until primary school. null France Individuals Patients population Male Female Infant, Newborn (birth to 28 days) Child (6 to 12 years) All participating newborns hospitalised by neonatal and paediatric neurology services. Full-term newborns presenting perinatal arterial ischaemic stroke were included i.e.: - presenting neurological symptoms (convulsions, malaise, hypotonia, impaired vigilance, asymmetric tone or motor skills) in the first 28 days of life; - Brain imaging (by CT or MRI scan) showing appearance of ischaemic-like lesions in an arterial location; - parents or those with parental authority who gave their consent after explanation of the protocol aims and modalities by the local investigating party and who received an explanatory document. premature births; - asymptomatic neonates i.e. systematic discovery of an immediate pre- or post-natal image abnormality or children presenting with aposteriori cerebral palsy; - children with diffuse hypoxic-ischaemic lesions i.e more than three affected arterial territories or venous infarction; - where clinical and biological follow-up is impossible; - parental refusal to be included in the study or refusal to sign molecular biology consent form. Clinical data Participant-reported health data Biological data Paraclinical data (non-biological) : Imaging Quality of life/health perception Other Through organizations (health services or institutions schools businesses etc.) < 500 individuals Self-administered questionnaire Interview with the participant (including clinical) Observational Study Observational Study 100 Unknown Restricted access Data may be used by academic teams To be decided if data may be used by industrial teams. Access on specific project only