Molecular basis of lymphatic dysplasia in children

Molecular basis of lymphatic dysplasia in children - DNALymph

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON38818

Enrollment

105

Registered

2013-08-30

Start date

2013-09-01

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

lymphedema

Interventions

None listed

Eligibility

Age

2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients * Diagnosed with lymphatic dysplasia in infancy or early childhood * Parents / caregivers of patients able to read and understand the written information Parents * Parents of patients with lymphatic dysplasia as a child * Able to read and understand the written information

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Detection of further gene(s) causing lymphatic dysplasia in children.	—

Secondary

Measure	Time frame
- Understanding the molecular and cellular mechanisms leading to the various manifestations of lymphatic dysplasia in children. - Increase of our understanding of lymph vessel formation in man	—

Countries

Netherlands

Outcome results