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

A male phenotype with Aicardi syndrome.

Journal of child neurology - 1 Feb 2009

Zubairi Mohammad S, Carter Ronald F, Ronen Gabriel M

Abstract excerpt

Aicardi syndrome is a rare neurodevelopmental condition that occurs almost exclusively in women. We report a second male phenotype and 47,XXY karyotype with a typical presentation of the Aicardi syndrome including a midline arachnoid cyst.

Read the complete abstract on PubMed

Topics

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

Share to Electroencephalography
Share to Seizures
Share to Tomography, X-Ray Computed

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Agenesis of Corpus Callosum

Share to Aneuploidy

Share to Chromosomes, Human, X

Share to Corpus Callosum

Share to Developmental Disabilities

Source

Identifiers

PMID: 19182158
DOI: 10.1177/0883073808322337

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A male phenotype with Aicardi syndrome.PMID 19182158Read ↗

Aicardi syndrome in a genotypic male.Semantic proximity Read ↗

Facial and physical features of Aicardi syndrome: infants to teenagers.Semantic proximity Read ↗

Aicardi syndrome in a male patient.Semantic proximity Read ↗

[Aicardi syndrome: retrospective study of a series of seven case reports].Semantic proximity Read ↗

Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and GeneticsSemantic proximity Read ↗

Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesisSemantic proximity Read ↗

[Clinical outcome of distinct Aicardi syndrome phenotypes].Semantic proximity Read ↗

Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children.Semantic proximity Read ↗

Central nervous system malformations in the CHARGE associationSemantic proximity Read ↗

Laryngomalacia, choanal atresia and renal anomaly in a newborn with Freeman-Sheldon syndrome phenotype.Semantic proximity Read ↗

AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.Semantic proximity Read ↗

Aicardi syndromeSemantic proximity Read ↗

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