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Diagnostics and diagnosis oriented research of mental retardation of unknown cause

Diagnostics and diagnosis oriented research of mental retardation of unknown cause - Diagnostics of mental retardation of unknown cause

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30801
Enrollment
400
Registered
2009-01-12
Start date
2009-07-14
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

mental handicap mental impairment

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: mental retardation of unknown origin availability of both parents additionnal features (e.g congenital malformations, dysmorphology, consanguinity, micro/macrocephaly, abnormal growth)

Exclusion criteria

Exclusion criteria: mental retardation of known cause

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is having a etiological diagnosis and establishing a genetic-diagnostic protocol to be used in the MR sector by the AVG.

Secondary

MeasureTime frame
Finding new genes and new MR syndromes are secundary outcome measures as are the genotype/phenotype correlation studies

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)