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.

Catastrophic Antiphospholipid Syndrome (CAPS) is a rare, severe autoimmune disease causing rapid-onset, widespread blood clotting and multi-organ failure. Prompt diagnosis and aggressive treatment are crucial for survival.

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.

Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder causing abnormal blood vessels, leading to frequent nosebleeds and internal bleeding.

Ehlers-Danlos Syndrome (EDS) is a genetic disorder characterized by joint hypermobility, skin elasticity, and often fragile tissues. It can cause pain, fatigue, and other complications.

An embolus is a traveling blood clot that can block blood flow, causing serious complications like pulmonary embolism or stroke. Early detection and treatment are crucial to prevent these life-threatening risks.