Clinical Interest of a Genetic Diagnosis in Early Infant Epilepsy, Paraclinical and Therapeutic Management, and Psychological Impact of Families

University Hospital, Strasbourg, France

Status: Not yet enrolling

Conditions: Early Infant Epilepsy

Treatments: Other: Questionnaires

Study type: Observational

Funder types: Other

Identifiers

NCT05455333

8609 (Other Identifier)

Details and patient eligibility

About

To determine the paraclinical and therapeutic interest of genetic diagnosis in early onset epilepsy.

Enrollment: 75 estimated patients

Sex: All

Ages: Under 12 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Children aged ≤ 12 years,
• hospitalized or followed at the Hautepierre Hospital of the University Hospitals of Strasbourg for primary epilepsy having started in the first 5 months of life, from 2010 to 2021.

Exclusion criteria

• Children with secondary epilepsy (with infection trauma)