G40 F45.0
Conditions
Interventions
Group 1: Clinical data and DNA samples will be collected continuously throughout the study period.
Sponsors
Universitätsklinikum der RWTH Aachen
Eligibility
Sex/Gender
All
Age
0 Years to 105 Years
Inclusion criteria
Inclusion criteria: - Individuals with diagnosis of epilepsy syndrome or related paroxysmal disorder - 1st and 2nd degree relatives of individuals with diagnosis of epilepsy syndrome or related paroxysmal disorder
Exclusion criteria
Exclusion criteria: Individuals who are not able to give informed consent by themselves or by a legal guardian
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Genetic analysis of collected samples. | — |
Secondary
| Measure | Time frame |
|---|---|
| Identification of genetic variants for further functional studies. | — |
Countries
Germany
Contacts
Public ContactStefan Wolking
Universitätsklinikum der RWTH Aachen
Outcome results
None listed