Molecular basis of Primrose syndrome

Molecular basis of Primrose syndrome - Molecular basis of Primrose syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON38472

Enrollment

Registered

2013-08-20

Start date

2013-09-10

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

Primrose syndrome

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For patients: Diagnosed with Primrose syndrome Parents/caregivers able to read and understand written information For parents: Parent of child diagnosed with Primrose syndrome Able to read and understand written information

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
Detection of the gene causing Primrose syndrome.	—

Secondary

Measure	Time frame
- Understanding the molecular and cellular mechanisms leading to the various manifestations of Primrose syndrome. - better understanding of the regulation of heterotopic calcifications	—

Countries

Netherlands

Outcome results