Epilepsy in patients with familial hemiplegic migraine.

Hasırcı Bayır B. R., Tutkavul K., Eser M., Baykan B.

Seizure, cilt.88, ss.87-94, 2021 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 88
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.seizure.2021.03.028
  • Dergi Adı: Seizure
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, CINAHL, EMBASE, MEDLINE, Psycinfo
  • Sayfa Sayıları: ss.87-94
  • Anahtar Kelimeler: Familial hemiplegic migraine, Epilepsy, Prognosis, Gene, Mutation, ATP1A2 GENE MUTATION, PAROXYSMAL DYSKINESIA, SPREADING DEPRESSION, CHILDHOOD EPILEPSY, FEBRILE SEIZURES, PRRT2 MUTATIONS, ILAE COMMISSION, PATHOPHYSIOLOGY, TYPE-2, SCN1A
  • İstanbul Üniversitesi Adresli: Evet

Özet

Objective: : The coexistence of epilepsy in familial hemiplegic migraine (FHM) has not been reviewed systematically. We investigated the associations of epilepsy in patients with FHM with CACNA1A, ATP1A2, SCN1A or PRRT2 mutations along with clinical and genetic data.