Congenital plasminogen activator inhibitor type 1 deficiency
- Synonyms
- HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY; Plasminogen activator inhibitor type 1 deficiency
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Meadow Heiman
- Sweta Gupta
- Magdalena Lewandowska
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Abnormal bleeding
Abnormal bleeding
- MedGen UID: 264316
- Concept ID: C1458140
- Finding: Pathologic Function
Abnormality of blood and blood-forming tissues
- Menorrhagia
Menorrhagia
- MedGen UID: 44358
- Concept ID: C0025323
- Finding: Pathologic Function
Abnormality of blood and blood-forming tissues
- Abnormal bleeding
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