Ring chromosome 20 syndrome: Electroclinical description of six patients and review of the literature-Reference-Cited by-同舟云学术

Ring chromosome 20 syndrome: Electroclinical description of six patients and review of the literature

Published:2012-04 Issue:4 Volume:23 Page:409-414
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Elens Iris,Vanrykel Katrien,De Waele Liesbeth,Jansen Katrien,Segeren Merel,Van Paesschen Wim,Ceulemans Berten,Boel Marc,Frijns Jean-Pierre,Buyse Gunnar,Lagae Lieven

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference25 articles.

1. Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients;Conlin;J Med Genet,2011

2. Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci;Elghezal;Eur J Med Genet,2007

3. Mosaic ring 20 with no detectable deletion by FISH analysis: characteristic seizure disorder and literature review;Zou;Am J Med Genet,2006

4. Catalogue of unbalanced chromosome aberrations in man;Schinzel,2001

5. Ring chromosome 20 epilepsy syndrome in children: electroclinical features;Serrano-Castro;Neurology,2002

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1. Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review;Genes;2023-01-23

2. Reflex seizures with hot water and recurrent nonconvulsive status epilepticus in a patient with triple mosaicism and ring formation of chromosome 20;Neurological Sciences and Neurophysiology;2022

3. Electroclinical Improvement in a Patient with Ring Chromosome 20 Syndrome Treated with Zonisamide: A Case Report;Journal of Pediatric Genetics;2021-04-01

4. A case of drug-resistant epilepsy associated with ring Chromosome 20;Annals of Indian Academy of Neurology;2021

5. Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes;Frontiers in Neurology;2020-12-08