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2019
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- handle: 10670/1.q61knw
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familial focal epilepsy with variable foci DEPDC5 semiology occipital seizure semiology frontal seizuresSujets proches
Semiology (Medicine) Diseases--Symptoms Symptomatology Signs, Clinical Clinical signs Semiology Symptomology Signs and symptoms Disease symptoms Searches and seizures--Law and legislation Seizures Family Family structure Families--Social aspects Families--Social conditions Family life Structure, Family Family relationships Relationships, Family Biography--Ancestry Relations with family Biography--Descendants Biography--Family AncestryCiter ce document
Marina Aberastury et al., « DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family », Epileptic Disorders, ID : 10670/1.q61knw
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AimsFamilial 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.