Journal de la Faculté de Médecine
Volume 1, Numéro 3, Pages 221-228

Polymorphismes Du Gène Reln Et Susceptibilité à L’épilepsie Et à La Schizophrénie : Etude Clinique Et Génétique D’une Famille Algérienne

Auteurs : Chentouf Amina . Ouabaiche Mohand-laid . Dahdouh Aicha . Salzmann Annick . Antonarakis Stylianos .


Abstract Introduction - Several studies have shown a strong relationship between schizophrenia and epilepsy. This association implies a common genetic susceptibility for both conditions. This study aims to identify genetic variants of susceptibility to epilepsy and schizophrenia in an Algerian family. Patients and methods - All available members of this family underwent clinical and electroencephalographic evaluation. Genetic analysis by whole exome sequencing was performed after DNA extraction. Results - In this study, we report a family with two brothers having temporal lobe epilepsy associated to schizophrenia in one, and to recurrent depressive disorder in the other. Exome sequencing identified homozygous single nucleotide variant in the RELN gene (rs55689103) in patient with schizophrenia. His brother was heterozygous for the same variant. Conclusion - The polymorphism rs55689103 could be involved in schizophrenic phenotype in this family, but not in epilepsy phenotype. Further investigations of blood Reelin level and RELN promoter methylation are key components to interpreting the results of this study.

Mots clés

Reelin, RELN, polymorphism, epilepsy, schizophrenia.

Prédisposition Génétique à La Néphropathie Diabétique: Rôle Du Polymorphisme I/d Du Gène Ace

Hanachi Sabah .  Sifi Karima .  Boudaoud Khalida .  Zekri Salima .  Houche Sara .  Houamel Hanane .  Hassini Soumia .  Benembarek Karima .  Abadi Nouredine . 
pages 541-548.

étude Clinique Et Génétique D’une Cohorte De 46 Patients Atteints D’ataxie De Friedreich

Ali Pacha L. .  Benhassine T. .  Assami S. .  Nouioua Samia .  Hamza W. .  Koenig M. .  Tazir M. . 
pages 32-39.