EVALUATION OF CLINICAL, DEMOGRAPHIC AND ELECTROENCEPHALOGRAPHY FINDINGS OF DRAVET SYNDROME PATIENTS

ASLAN, MAHMUT; GÜNGÖR, SERDAL

doi:10.26650/iuitfd.2019.0024

EVALUATION OF CLINICAL, DEMOGRAPHIC AND ELECTROENCEPHALOGRAPHY FINDINGS OF DRAVET SYNDROME PATIENTS

Atıf İçin Kopyala

ASLAN M., GÜNGÖR S.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.84, sa.1, ss.64-67, 2021 (ESCI)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 84 Sayı: 1
Basım Tarihi: 2021
Doi Numarası: 10.26650/iuitfd.2019.0024
Dergi Adı: JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), TR DİZİN (ULAKBİM)
Sayfa Sayıları: ss.64-67
İnönü Üniversitesi Adresli: Evet

Özet

Objective: Dravet syndrome (DS) is a severe myoclonic epilepsy affecting infants and is classified among epileptic syndromes. Generally, the first seizures begin with febrile diseases during infancy. Cognitive functions and behavior of patients begin to decline from the age of two. In DS, the most common SCN1A mutation is detected.