congenital prothrombin deficiency

Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.

What is congenital prothrombin deficiency?

congenital prothrombin 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 prothrombin deficiency, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with congenital prothrombin deficiency

Bruising susceptibilityEpistaxisGastrointestinal hemorrhageGingival bleedingJoint hemorrhageMenorrhagiaProlonged bleeding time

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.