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Identification of genetic causes and designed therapy by large sized exome data establishment in Charcot-Marie-Tooth disease

Identification of genetic causes and designed therapy by large sized exome data establishment in Charcot-Marie-Tooth disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0000369
Enrollment
220
Registered
2012-02-24
Start date
2011-11-07
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Ewha Womans University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Neuropathic findings by clinical neurological examination 2. Peripheral neurpopathy confirmed by electrophisiological test 3. Existence of family history or suspect by genetic disease

Exclusion criteria

Exclusion criteria: 1. Identification of the cause of neuropahty 2. Confirmed of symptoms by acquired neuropathy 3. No family history or condsideration of the disease with genetic causes

Design outcomes

Primary

MeasureTime frame
gene mutation—

Secondary

MeasureTime frame
polkymorphism—

Countries

Korea, Republic of

Contacts

Public ContactYun Yoo

Ewha Womans University Medical Center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026