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

Seizures and X-linked intellectual disability.

European journal of medical genetics - 1 May 2012

Stevenson Roger E, Holden Kenton R, Rogers R Curtis, Schwartz Charles E

Abstract excerpt

Intellectual disability occurs as an isolated X-linked trait and as a component of recognizable X-linked syndromes in the company of somatic, metabolic, neuromuscular, or behavioral abnormalities. Seizures accompany intellectual disability in almost half of these X-linked disorders. The spectrum...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Brain
Share to Epilepsy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Metabolism, Inborn Errors

Share to Phenotype

Share to Syndrome

Share to X-Linked Intellectual Disability

Source

Open in PubMed Open full text

Identifiers

PMID: 22377486
DOI: 10.1016/j.ejmg.2012.01.017
PMCID: PMC3531238

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22377486-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Seizures and X-linked intellectual disability.PMID 22377486Read ↗

Genetics, molecular biology, and phenotypes of x-linked epilepsy.Semantic proximity Read ↗

The molecular and phenotypic spectrum of IQSEC2-related epilepsy.Semantic proximity Read ↗

Phenotypic spectrum of SETD1B-related disorder: Myoclonic absence seizures and concurrent intellectual disability - Insights from two cases.Semantic proximity Read ↗

The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizures.Semantic proximity Read ↗

Protocadherin 19 mutations in girls with infantile-onset epilepsySemantic proximity Read ↗

Genes and loci involved in febrile seizures and related epilepsy syndromes.Semantic proximity Read ↗

A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity.Semantic proximity Read ↗

Delineating the epilepsy phenotype of NGLY1 deficiency.Semantic proximity Read ↗

Epilepsy and autism: neurodevelopmental perspective.Semantic proximity Read ↗

Novel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4.Semantic proximity Read ↗

X-linked myoclonic epilepsy with spasticity and intellectual disabilitySemantic proximity Read ↗

The Broad Clinical Spectrum of Epilepsies Associated With Protocadherin 19 Gene MutationSemantic proximity Read ↗

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