Book contents
- Frontmatter
- Contents
- List of Contributors
- Preface to the Second Edition
- Preface to the First Edition – an Act of Supererogation?
- Abbreviations
- Section I Introduction
- Section II Approaches to the Clinical Investigation and Diagnosis of Cause
- Section III Idiopathic Epilepsies
- Section IV Symptomatic Epilepsies of Genetic or Developmental Origin
- (a) Single Gene Disorders and Inborn Errors of Metabolism
- 16 Benign Familial Neonatal Epilepsy (BFNE)
- 17 Sleep-Related Hypermotor Epilepsy (SHE)
- 18 Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- 19 Dravet Syndrome and Other SCN1A Disorders
- 20 Familial Lateral Temporal Lobe Epilepsy
- 21 Familial Focal Epilepsy with Variable Foci
- 22 PCDH19 Mutations Related Epilepsy: Phenotype and Genotype
- 23 CDKL5 Encephalopathy
- 24 KCNQ2 Encephalopathy
- 25 FOXG1 Encephalopathy
- 26 STXBP1 Encephalopathy
- 27 Rett Syndrome
- 28 Epilepsy and GLUT1 DS
- 29 Other Rare Single-Gene Disorders Causing Epileptic Encephalopathy
- 30 Mitochondrial Epilepsies
- 31 Lysosomal Disorders and Epilepsy
- 32 Peroxisomal Disorders and Epilepsy
- 33 Menkes’ Disease
- 34 Neuroacanthocytosis
- 35 Organic Acid and Amino Acid Metabolism Disorders
- 36 Porphyrias
- 37 Pyridoxine-Dependent Epilepsy
- 38 Fatty Acid Oxidation Disorders
- 39 GABA Syndromes
- 40 Disorders of Creatine Metabolism and Epilepsy
- 41 Epilepsy Caused by Congenital Disorders of Glycosylation
- 42 Urea Cycle Disorders
- 43 Hyperinsulinism–Hyperammonemia and Biotin Pathway Defects
- 44 Other Single-Gene Disorders
- (b) Progressive Myoclonic Epilepsies
- (c) Neurocutaneous Syndromes
- (d) Epilepsies Associated with Chromosomal Abnormalities
- (e) Epilepsies Associated with Developmental Anomalies of Cerebral Structure
- Section V Symptomatic Epilepsies of Acquired Origin
- Section VI Provoking Factors and Provoked Epilepsies: Reflex Seizures
- Section VII Status Epilepticus
- Index
16 - Benign Familial Neonatal Epilepsy (BFNE)
from (a) - Single Gene Disorders and Inborn Errors of Metabolism
Published online by Cambridge University Press: 12 April 2019
Book contents
- Frontmatter
- Contents
- List of Contributors
- Preface to the Second Edition
- Preface to the First Edition – an Act of Supererogation?
- Abbreviations
- Section I Introduction
- Section II Approaches to the Clinical Investigation and Diagnosis of Cause
- Section III Idiopathic Epilepsies
- Section IV Symptomatic Epilepsies of Genetic or Developmental Origin
- (a) Single Gene Disorders and Inborn Errors of Metabolism
- 16 Benign Familial Neonatal Epilepsy (BFNE)
- 17 Sleep-Related Hypermotor Epilepsy (SHE)
- 18 Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- 19 Dravet Syndrome and Other SCN1A Disorders
- 20 Familial Lateral Temporal Lobe Epilepsy
- 21 Familial Focal Epilepsy with Variable Foci
- 22 PCDH19 Mutations Related Epilepsy: Phenotype and Genotype
- 23 CDKL5 Encephalopathy
- 24 KCNQ2 Encephalopathy
- 25 FOXG1 Encephalopathy
- 26 STXBP1 Encephalopathy
- 27 Rett Syndrome
- 28 Epilepsy and GLUT1 DS
- 29 Other Rare Single-Gene Disorders Causing Epileptic Encephalopathy
- 30 Mitochondrial Epilepsies
- 31 Lysosomal Disorders and Epilepsy
- 32 Peroxisomal Disorders and Epilepsy
- 33 Menkes’ Disease
- 34 Neuroacanthocytosis
- 35 Organic Acid and Amino Acid Metabolism Disorders
- 36 Porphyrias
- 37 Pyridoxine-Dependent Epilepsy
- 38 Fatty Acid Oxidation Disorders
- 39 GABA Syndromes
- 40 Disorders of Creatine Metabolism and Epilepsy
- 41 Epilepsy Caused by Congenital Disorders of Glycosylation
- 42 Urea Cycle Disorders
- 43 Hyperinsulinism–Hyperammonemia and Biotin Pathway Defects
- 44 Other Single-Gene Disorders
- (b) Progressive Myoclonic Epilepsies
- (c) Neurocutaneous Syndromes
- (d) Epilepsies Associated with Chromosomal Abnormalities
- (e) Epilepsies Associated with Developmental Anomalies of Cerebral Structure
- Section V Symptomatic Epilepsies of Acquired Origin
- Section VI Provoking Factors and Provoked Epilepsies: Reflex Seizures
- Section VII Status Epilepticus
- Index
- Type
- Chapter
- Information
- The Causes of EpilepsyCommon and Uncommon Causes in Adults and Children, pp. 143 - 153Publisher: Cambridge University PressPrint publication year: 2019