Congenital plasminogen activator inhibitor type 1 deficiency

Congenital plasminogen activator inhibitor type 1 deficiency is a medical condition that may be associated with various symptoms and signs.

What is Congenital plasminogen activator inhibitor type 1 deficiency?

Congenital plasminogen activator inhibitor type 1 deficiency is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have Congenital plasminogen activator inhibitor type 1 deficiency, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with Congenital plasminogen activator inhibitor type 1 deficiency

EpistaxisGastrointestinal hemorrhageIntracranial hemorrhageJoint hemorrhageMenorrhagiaOral bleedingPersistent bleeding after traumaPost-partum hemorrhageProlonged bleeding after dental extractionProlonged bleeding after surgerySubcutaneous hemorrhage

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.