Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X region.

Neuropediatrics - 1 Aug 1993

Rees M, Diebold U, Parker K, Doose H, Gardiner R M, Whitehouse W P

Abstract excerpt

Benign childhood epilepsy with centrotemporal spikes (BCECS, benign rolandic epilepsy) is a common form of genetically determined localisation-related epilepsy of childhood. The characteristic age-dependent focal sharp wave (fsw) found on the EEG in this disorder segregates as a dominant trait in families with probands with BCECS. Seizures occur in a significant proportion of individuals with the fragile X...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Child
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genetic Linkage

Share to Genetic Markers

Share to Pedigree

Share to Phenotype

Source

Identifiers

PMID: 8232779
DOI: 10.1055/s-2008-1071542

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X region.PMID 8232779Read ↗

Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp waves.Semantic proximity Read ↗

Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population.Semantic proximity Read ↗

The genetics of rolandic epilepsy.Semantic proximity Read ↗

Children with Focal Sharp Waves: Clinical and Genetic AspectsSemantic proximity Read ↗

A microRNA‐328 binding site in<i>PAX6</i>is associated with centrotemporal spikes of rolandic epilepsySemantic proximity Read ↗

Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions.Semantic proximity Read ↗

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.Semantic proximity Read ↗

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).Semantic proximity Read ↗

Centrotemporal spikes in families with rolandic epilepsySemantic proximity Read ↗

Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families.Semantic proximity Read ↗

Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2Semantic proximity Read ↗

Epilepsy in fragile X syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.