Hemostasis Disorders

Hemophilia C

Discover how Hemophilia C (Factor XI deficiency) differs from types A and B, including its unique symptoms, diagnosis, and modern care.

Hemophilia B

Hemophilia B is a rare, inherited bleeding disorder caused by a lack of Factor IX. Modern treatments now include non-factor and gene therapies

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.

Thrombophilia

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.

Antiphospholipid Syndrome

Antiphospholipid Syndrome

Antiphospholipid syndrome (APS) is an autoimmune disorder that increases the risk of blood clots, pregnancy complications, and other health problems. Early diagnosis and management are crucial.

Secret Link