Is benign familial neonatal KCNQ2-related epilepsy always familially benign?
A 1-year-old infant was referred for a diagnostic work-up, due to a past history of generalized clonic seizures migrating from one side of the body to the other side, of short duration, and presenting in cluster, occurred in the first days of life. He is a component a large family in whom several me...
Main Authors: | Piero Pavone, Andrea D. Praticò, Raffaele Falsaperla, Pasquale Striano, Martino Ruggieri |
---|---|
Format: | Article |
Language: | English |
Published: |
Hygeia Press di Corridori Marinella
2018-08-01
|
Series: | Journal of Pediatric and Neonatal Individualized Medicine |
Subjects: | |
Online Access: | https://www.jpnim.com/index.php/jpnim/article/view/678 |
Similar Items
-
A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data
by: Gianluigi Laccetta, et al.
Published: (2019-09-01) -
Severe neonatal epileptic encephalopathy and KCNQ2 mutation: neuropathological substrate?
by: Charlotte eDalen Meurs-Van Der Schoor
Published: (2014-12-01) -
Deletion of KCNQ2/3 potassium channels from PV+ interneurons leads to homeostatic potentiation of excitatory transmission
by: Heun Soh, et al.
Published: (2018-11-01) -
Capturing seizures in clinical trials of antiseizure medications for KCNQ2‐DEE
by: John J. Millichap, et al.
Published: (2021-03-01) -
Behavioral and neuro-functional consequences of eliminating the KCNQ3 GABA binding site in mice
by: Kiki J. Chen, et al.
Published: (2023-05-01)