Genetic mutational analyses in hereditary skin diseases of minors

Genetic mutational analyses in hereditary skin diseases of minors - Genetic analyses in hereditary skin diseases of minors

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000006317

Enrollment

Registered

2011-10-30

Start date

2011-11-01

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

Hereditary skin disease

Interventions

10ml of blood sample is collected by venipuncture

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients under the age of 20 with hereditary skin diseases who or whose parent(s) understand the meaning of genetic analyses and give their consent to the study

Exclusion criteria

Exclusion criteria: Patients under the age of 20 with hereditary skin diseases who or whose parent(s) cannot understand the meaning of genetic analyses nor give their consent to the study.

Design outcomes

Primary

Measure	Time frame
Genetic analyses will be completed from the patient's blood sample in several months.	—

Secondary

Measure	Time frame
It will take more months to finish if the first genetic analyses fail to identify the causative gene or mutational site.	—

Countries

Japan

Contacts

Public ContactWataru Fujimoto

Kawasaki Medical School Department of Dermatology

watarufu@med.kawasaki-m.ac.jp086-462-1111

Outcome results

None listed

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