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The clinical features and causative genes of Familial idiopathic basal ganglia calcification (Fahr's disease)

The clinical features and causative genes of Familial idiopathic basal ganglia calcification (Fahr's disease)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-COC-15006713
Enrollment
Unknown
Registered
2015-07-07
Start date
2015-07-10
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Familial Idiopathic Basal Ganglia Calcification

Interventions

Patients from 20 Families and normal person:no

Sponsors

Department of Clinical Pharmacology, Xiangya Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 85 Years

Inclusion criteria

Inclusion criteria: Familial Idiopathic Basal Ganglia Calcification families.

Exclusion criteria

Exclusion criteria: Patients with secondary basal ganglia calcification.

Design outcomes

Primary

MeasureTime frame
gene;—

Secondary

MeasureTime frame
volume of Basal ganglia calcification;onset age;sex;Clinical symptoms;—

Countries

China

Contacts

Public ContactHong-Hao Zhou
hhzhou2003@163.com+86 0731-84805379

Outcome results

None listed

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