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Molecular mechanisms of LRSAMI gene mutations causing Charcot-Marie-Tooth patients

Molecular mechanisms of LRSAMI gene mutations causing Charcot-Marie-Tooth patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097417
Enrollment
Unknown
Registered
2025-02-19
Start date
2024-07-18
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Charcot-Marie-Tooth disease type 2P

Interventions

Observation group:None

Sponsors

Fuzhou University Affiliated Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The families of patients clinically diagnosed with CMT2P in the Provincial Hospital of Fuzhou University in November 2022 were selected as the research subjects

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Physical examination of the nervous system and neuroelectrophysiological examination;

Secondary

MeasureTime frame
Charcot-Marie-Tooth Neuropathy Score, CMTNS;

Countries

China

Contacts

Public ContactJiang Ying

Fuzhou University Affiliated Provincial Hospital

jy-meave@163.com+86 158 8010 0211

Outcome results

None listed

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