Study on susceptibility genes for SMON

Study on susceptibility genes for SMON - Study on susceptibility genes for SMON

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000023797

Enrollment

100

Registered

2017-12-01

Start date

2016-09-01

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

SMON(subacute myelo-optico-neuropathy)

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Diagnosed as having SMON

Exclusion criteria

Exclusion criteria: Non-SMON

Design outcomes

Primary

Measure	Time frame
Allele frequency of C609T of NQO1 gene	—

Countries

Japan

Contacts

Public ContactToshiyuki Fukao

Graduate school of medicine, Gifu University Department of Pediatrics

toshi-gif@umin.net058-230-6380

Outcome results