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

The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.

Developmental disabilities research reviews - 1 Jan 2009

Boada Richard, Janusz Jennifer, Hutaff-Lee Christa, Tartaglia Nicole

Abstract excerpt

Klinefelter syndrome (KS) or 47,XXY occurs in approximately 1 in 650 males. Individuals with KS often present with physical characteristics including tall stature, hypogonadism, and fertility problems. In addition to medical findings, the presence of the extra X chromosome can lead to characteristic cognitive and language deficits of varying severity. While a small, but significant downward shift in mean overall...

Read the complete abstract on PubMed

Topics

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

Share to Attention
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cognition Disorders

Share to Klinefelter Syndrome

Share to Language Disorders

Share to Neuropsychological Tests

Share to Space Perception

Share to Visual Perception

Source

Open in PubMed Open full text

Identifiers

PMID: 20014369
DOI: 10.1002/ddrr.83
PMCID: PMC3056507

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

The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.PMID 20014369Read ↗

Klinefelter Syndrome: Integrating Genetics, Neuropsychology, and EndocrinologySemantic proximity Read ↗

Neurobehavioral phenotype of Klinefelter syndrome.Semantic proximity Read ↗

New Horizons in Klinefelter Syndrome: Current Evidence, Gaps, and Research PrioritiesSemantic proximity Read ↗

An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.Semantic proximity Read ↗

Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations.Semantic proximity Read ↗

Neuropsychology and brain morphology in Klinefelter syndrome - the impact of genetics.Semantic proximity Read ↗

Neuropsychiatric Aspects in Men with Klinefelter Syndrome.Semantic proximity Read ↗

International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences.Semantic proximity Read ↗

Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome)Semantic proximity Read ↗

Advances in research on the neurological and neuropsychiatric phenotype of Klinefelter syndrome.Semantic proximity Read ↗

Klinefelter Syndrome. The Effects of Early Androgen Therapy on Competence and Behavioral Phenotype.Semantic proximity Read ↗

Neuropsychological Findings in Adults with Triple X SyndromeSemantic proximity Read ↗

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