Study of phenotype in Silver-Russell syndrome patients with known molecular abnormalities

Study of phenotype in Silver-Russell syndrome patients with known molecular abnormalities - Silver-Russell syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON32891

Enrollment

Registered

2009-01-19

Start date

2008-09-01

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

Silver-Russell syndrome

Interventions

None listed

Eligibility

Age

2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Silver-Russell syndrome, proven by DNA analysis (either uniparental disomy 7 or hypomethylation H19)

Exclusion criteria

Exclusion criteria: non-cooperation of patient or parents

Design outcomes

Primary

Measure	Time frame
growth; phsyical characteristics	—

Secondary

Measure	Time frame
other health problems	—

Countries

Netherlands

Outcome results