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.

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.

Hemophilia A

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.

Bernard-Soulier Syndrome

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.

Bernard-Soulier Syndrome

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.

Purpura

Purpura

Purpura: Purple skin spots from bleeding. Learn about causes (low platelets, vessels), and symptoms.

Ecchymoses

Ecchymoses

Ecchymoses, or bruises, are skin discolorations from blood leakage. Causes range from minor injury to underlying medical issues. Understanding them is key.

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