Molecular Basis of Parry-Romberg syndrome

Molecular Basis of Parry-Romberg syndrome - Molec Parry-Romberg

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON37608

Enrollment

Registered

2012-04-11

Start date

2012-04-11

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

Progressive hemifacial atrophy

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Diagnosed with Parry-Romberg syndrome * Patients able to read and understand the written information * 18 years of age or older

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
Detection of the gene causing Parry-Romberg syndrome.	—

Secondary

Measure	Time frame
Understanding of the molecular and cellular mechanisms leading to the various manifestations of Parry-Romberg syndrome.	—

Countries

Netherlands

Outcome results