A Clinical, Molecular Genetic and Coagulation study in patients with Klippel-Trenaunay Syndrome and related entities

A Clinical, Molecular Genetic and Coagulation study in patients with Klippel-Trenaunay Syndrome and related entities - Klipple-Trenaunay syndrome

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON35243

Enrollment

Registered

2011-10-25

Start date

2011-09-01

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Klippel-Trenaunay syndrome

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Diagnosis Klippel-Trenaunay syndrome Age >18yr

Exclusion criteria

Exclusion criteria: Unreliable diagnosis Age

Design outcomes

Primary

Measure	Time frame
Detection of AKT1 gene mutations	—

Secondary

Measure	Time frame
none	—

Countries

Netherlands

Outcome results