Platelet Disorders

Hemophilia A

Hemophilia A is an X-linked bleeding disorder from a Factor VIII deficiency. It causes deep joint bleeds and is managed by FVIII replacement or gene therapy.

Factor V Leiden Thrombophilia

An inherited blood clotting disorder, Factor V Leiden increases your risk of developing dangerous clots like DVT and PE.

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.

Glanzmann Thrombasthenia

Glanzmann Thrombasthenia

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

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