Platelet Disorders

Coagulation Screening Panel Interpretation (Coagulation Panel)

A coagulation screening panel is a vital diagnostic tool. It assesses blood clotting (hemostasis) via PT, aPTT, & platelet count, revealing bleeding or clotting risks.

Glanzmann Thrombasthenia

Glanzmann thrombasthenia (GT) is a rare genetic bleeding disorder. Defective platelet aggregation leads to mucocutaneous bleeding. Diagnosis involves specialized lab tests.

Bernard-Soulier Syndrome

Bernard-Soulier Syndrome (BSS) is a rare inherited bleeding disorder characterized by enlarged platelets, low platelet count, and defective platelet function, often presenting in infancy or early childhood.

Thrombophilia

Thrombophilia is an increased tendency to form blood clots. It can be inherited or acquired, raising the risk of DVT, PE, and other thrombotic events. Understanding its causes and management is crucial.

Fibrinolysis

Fibrinolysis

The process of fibrinolysis dissolves fibrin clots after wound healing, restoring blood flow and preventing unwanted thrombus formation.

Venous Thrombosis (VTE)

Venous Thrombosis (VTE)

Venous thromboembolism: Unilaterla leg pain with lungs at risk. Master Virchow’s triad (stasis, hypercoagulability, injury), recognize DVT & PE, and advocate for early diagnosis & prevention.