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
- (b) Progressive Myoclonic Epilepsies
- (c) Neurocutaneous Syndromes
- (d) Epilepsies Associated with Chromosomal Abnormalities
- 56 Copy Number Variations Causing Epilepsy
- 57 MECP2 Duplication Syndrome
- 58 Down Syndrome
- 59 Fragile X Syndrome
- 60 4p Deletion (Wolf–Hirschhorn) Syndrome
- 61 Inverted Duplicated Chromosome 15 (Isodicentric Chromosome 15)
- 62 Ring Chromosome 20
- 63 Ring Chromosome 14 and Other Rare Ring Chromosomal Disorders
- 64 Angelman Syndrome
- (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
62 - Ring Chromosome 20
from (d) - Epilepsies Associated with Chromosomal Abnormalities
Published online by Cambridge University Press: 12 April 2019
- 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
- (b) Progressive Myoclonic Epilepsies
- (c) Neurocutaneous Syndromes
- (d) Epilepsies Associated with Chromosomal Abnormalities
- 56 Copy Number Variations Causing Epilepsy
- 57 MECP2 Duplication Syndrome
- 58 Down Syndrome
- 59 Fragile X Syndrome
- 60 4p Deletion (Wolf–Hirschhorn) Syndrome
- 61 Inverted Duplicated Chromosome 15 (Isodicentric Chromosome 15)
- 62 Ring Chromosome 20
- 63 Ring Chromosome 14 and Other Rare Ring Chromosomal Disorders
- 64 Angelman Syndrome
- (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. 435 - 438Publisher: Cambridge University PressPrint publication year: 2019