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Development of the genetic diagnosis system of congenital and Inherited skin disorders

Development of the genetic diagnosis system of congenital and Inherited skin disorders - Development of the genetic diagnosis system of congenital and Inherited skin disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000009851
Enrollment
8050
Registered
2013-01-25
Start date
2013-01-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

congenital and Inherited skin disorders

Interventions

None listed

Sponsors

Department of Dermatology, Keio University School of Medicine
Lead Sponsor
National Center for Child Health and Development
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having skin diseases that could be congenital or inherited

Exclusion criteria

Exclusion criteria: Having non-congenital skin disorder

Design outcomes

Primary

MeasureTime frame
By this method, we can analyze multiple gene mutations by a single analysis.

Countries

Japan,Asia(except Japan)

Contacts

Public ContactAkiharu Kubo

Keio University School of Medicine Department of Dermatology

akiharukubo@gmail.com03-3353-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026