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Genetic analysis of short stature

Genetic analysis of short stature - Genetic analysis of short stature

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30788
Enrollment
150
Registered
2009-02-04
Start date
2009-06-29
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

dwarfism shortness

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with short stature and their parents

Exclusion criteria

Exclusion criteria: No permission; biological parents not available; medical information of the patient not available; known diagnosis, confirmed by molecular, cytogenetic or cytological analysis

Design outcomes

Primary

MeasureTime frame
a. diagnostic possibilities in patients with short stature b. genetic factors which are involved in short stature with or without disproportion c. the potential value of proteomics techniques in the diagnostic process of short stature.

Secondary

MeasureTime frame
Not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)