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

Aarskog syndrome: the changing phenotype with age.

American journal of medical genetics - 1 Jan 2000

Fryns J P

Abstract excerpt

We describe the Leuven experience with 52 males with Aarskog syndrome particularly with respect to clinical variability, changing phenotype with age, and previously unreported signs. At least 30% of affected males were mentally retarded, two thirds of them at the level of slight mental handicap. Hyperactive behavior and symptoms of attention deficit disorders were frequently observed (61% of the mentally normal...

Topics

Adolescent
Adult
Aging
Child
Child, Preschool
Face
Genetic Linkage
Genitalia, Male
Humans
Intellectual Disability
Intelligence
Male
Mental Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Syndrome

X Chromosome

Source

Identifiers

PMID: 1605221
DOI: 10.1002/ajmg.1320430164

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1605221-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Aarskog syndrome: the changing phenotype with age.PMID 1605221Read ↗

Klinefelter syndrome: clinical and molecular aspects.Semantic proximity Read ↗

Helsmoortel-Van der Aa syndrome – psychophysical functioning of patient and therapeutic management (case report)Semantic proximity Read ↗

Neuropsychiatric findings of Möbius sequence – a reviewSemantic proximity Read ↗

Angelman syndrome: evolution of the phenotype in adolescents and adults.Semantic proximity Read ↗

Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.Semantic proximity Read ↗

[Aarskog syndrome. A case report].Semantic proximity Read ↗

Motor and behavioral phenotype of Dravet syndrome in adulthood.Semantic proximity Read ↗

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.Semantic proximity Read ↗

Another adult with Meier-Gorlin syndrome--insights into the natural history.Semantic proximity Read ↗

Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome).Semantic proximity Read ↗

A genetic diagnostic survey in an institutionalized population of 116 moderately to severely retarded male patients: the Rekem experience.Semantic proximity Read ↗

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