Primary Lymphedema and Mutation CELSR1 (Cadherin EGF LAG Seven-pass G-type Receptor 1)

NCT ID: NCT04919655

Last Updated: 2021-06-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

31 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-02-01

Study Completion Date

2022-02-20

Brief Summary

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The investigators will describe the expression of mutation CELSR1 with codon stop and amino acids substitution mechanism in primary lymphedema, in both clinical examination and imaging exploration

Detailed Description

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According to the literature, it seems that the mutation of the CELSR1 gene is associated with primary lymphedema.

Thus, the investigators have identified families with CELSR1 mutation with codon stop or animo acid substitution mechanisms among patients followed up in vascular medicine department, at Montpellier University hospital for primary lymphedema of lower limbs.

Among the mutation carriers, the investigators have collected the clinical examinations and imaging exploration results, realized systematically during the follow up of all the patient with primary lymphedema (venous Doppler, MRI of the lymphatic system, lymphoscintigraphy of the lower limbs, abdominal ultrasound), in order to search for a morphological and functional pattern associated with the mutation.

Conditions

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Primary Lymphedema

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patient followed up in vascular medicine departement at Montpellier University Hospital for primary lymphedema of lower limbs, who carries the CELSR1 mutation with codon stop or amino acids substitution mechanism.
* Relatives to the index case who carry the mutation for the segregation study.

Exclusion Criteria

* Patients who carry another mutation than CELSR1 responsible for primary lymphedema
* Syndromic form of primary lymphedema
* Patient not followed up at Montpellier University Hospital.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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GEHU - Duve Institute - Bruxelles

UNKNOWN

Sponsor Role collaborator

University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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MESTRE GODIN Sandrine

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Montpellier

Locations

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Uhmontpellier

Montpellier, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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MESTRE GODIN Sandrine, MD, PhD

Role: CONTACT

467337028 ext. 33

Aurélie LAY, résident

Role: CONTACT

4 67 33 70 28 ext. 33

Facility Contacts

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MESTRE GODIN Sandrine

Role: primary

467337028 ext. 33

Stéphanie BADOUAILLE

Role: backup

4 67 33 70 28 ext. 33

Other Identifiers

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RECHMPL21_0086

Identifier Type: -

Identifier Source: org_study_id

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