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DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family Volume 21, issue 1, February 2019

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  • DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family

Figures


  • Figure 1

  • Figure 2
Authors
1 Division of Neuropediatrics, Italian Hospital of Buenos Aires, CABA
2 Consultorio y laboratorio de Neurogenética, Centro Universitario de Neurología “J.M. Ramos Mejía” and División Neurología, Hospital JM Ramos Mejía, Facultad de Medicina, UBA, CABA
3 IBCN Eduardo de Robertis, Facultad de Medicina, UBA-CONICET, CABA
4 Bahía Blanca Italian Hospital, Bahía Blanca, Buenos Aires
5 Neurología Infantil, Hospital Italiano de Buenos Aires, CABA, Argentina
* Correspondence: Marina Aberastury Division of Neuropediatrics, Italian Hospital of Buenos Aires, 4135 Potosí St., CABA Argentina

Aims

Familial focal epilepsy with variable foci is a relatively rare autosomal disease with an unclear incidence, which is characterized by focal seizures arising from different cortical regions in different family members.