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Autism: from phenotype to genotype and back

Autism: from phenotype to genotype and back - Genes of Autism

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON41644
Enrollment
4500
Registered
2015-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism spectrum disorders Pervasive developmental disorders

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: The diagnosis of ASD in the proband, according to the DSM-IV (APA 1994) or DSM-5criteria, established by an expert clinician. Proband age between 5 and 25 years. Availability of at least 1 biological parent

Exclusion criteria

Exclusion criteria: Proband younger than 5 or older than 25 years of age. Family members of the proband: no age exclusion criteria. Epilepsy and/or mental retardation are not criteria for exclusion Known genetic disorders at entry (e.g. fragile X) are not a reason for exclusion, however such conditions will be noted in the participant*s research file.

Design outcomes

Primary

MeasureTime frame
(1) Non-synonymous single nucleotide changes in DNA coding sequence (2) Copy number variants

Secondary

MeasureTime frame
(1) Nature and severity of autistic symptoms (2) Nature and severity of co-morbid psychiatric symptoms Potential confounding factors including age, gender, years and level of education, years and level of parental education, medication use.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)