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Identification of White sponge nevus syndrome.

Identification of White sponge nevus syndrome. - White Sponge Naevus syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37321
Enrollment
25
Registered
2012-10-03
Start date
2012-10-10
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

Cannon's disease WSN

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Family members of this family with WSN. Also new subjects with signs of WSN in their family.

Exclusion criteria

Exclusion criteria: Legal incapacity.

Design outcomes

Primary

MeasureTime frame
The primary study parameter is a mutation in the keratinine 13-gene. To document phenotypical signs of of soft, white and spongy plaques in the (oral) mucosa, or extra-oral lesions. DNA-test can also be offered to subjects without phenotyipical signs of WSN.

Secondary

MeasureTime frame
not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)