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Genetic and molecular-biological study of hereditary coagulopathy

Not Applicable
Recruiting
Conditions
hereditary coagulopathy
Registration Number
JPRN-UMIN000003446
Lead Sponsor
Kobe University
Brief Summary

Fifty cases were investigated for AT deficiency and PS deficiency.

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
25
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who do not agree with genetic analysis.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Identification of genetic abnormality and molecular abnormality
Secondary Outcome Measures
NameTimeMethod
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