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

Migrating partial seizures in infancy and 47XYY syndrome: Cause or coincidence?

1 Jan 2014

Abstract excerpt

Migrating partial seizures in infancy (MPSI) is a rare epilepsy syndrome with poor prognosis. The exact etiology of MPSI is still not known. We report a 14-month-old baby with 47XYY karyotype who presented with developmental delay and drug-refractory seizures satisfying the diagnostic criteria for MPSI and discuss the possible association between the 47XYY karyotype and this syndrome. The excess of genes due to...

Read the complete abstract on PubMed

Topics

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

Share to Epilepsy research and treatment
Share to Genetics and Neurodevelopmental Disorders
Share to Genomic variations and chromosomal abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25667867
DOI: 10.1016/j.ebcr.2014.02.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Migrating partial seizures in infancy and 47XYY syndrome: Cause or coincidence?PMID 25667867Read ↗

X-linked neuronal migration disorders: Gender differences and insights for genetic screening.Semantic proximity Read ↗

Neuronal migration disorders, genetics, and epileptogenesis.Semantic proximity Read ↗

Interneuronopathies and their role in early life epilepsies and neurodevelopmental disordersSemantic proximity Read ↗

New trends in neuronal migration disorders.Semantic proximity Read ↗

A Case of Unilateral Closed-lip Schizencephaly Combined with Hypomyelination In NeonateSemantic proximity Read ↗

Migrating partial seizures in infancy: expanding the phenotype of a rare seizure syndrome.Semantic proximity Read ↗

Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis SyndromeSemantic proximity Read ↗

<i>SLC25A22</i>is a novel gene for migrating partial seizures in infancySemantic proximity Read ↗

Lissencephaly and Other Malformations of Cortical Development: 1995 UpdateSemantic proximity Read ↗

Basic mechanisms of catastrophic epilepsy -- overview from animal models.Semantic proximity Read ↗

X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".Semantic proximity Read ↗

Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.Semantic proximity Read ↗

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