| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8812835 | The Journal of Pediatrics | 2017 | 5 Pages |
Abstract
KCNT1 mutations are gain-of-function mutations in potassium channels resulting in severe infantile epilepsy. Herein we describe 3 infants with malignant migrating partial seizures with KCNT1 mutations accompanied by massive systemic to pulmonary collateral arteries with life-threatening hemoptysis and heart failure.
Related Topics
Health Sciences
Medicine and Dentistry
Perinatology, Pediatrics and Child Health
Authors
Yuki MD, Ichiro MD, Eiji MD, Yosuke MD, Shin MD, Hisashi MD, Munetsugu MD, PhD, Yoriko MD, PhD, Shintaro MD, PhD, Kenji MD, PhD, Hirotomo MD, PhD, Naomichi MD, PhD,