HELLP syndrome: A serious pregnancy issue with hemolysis, elevated liver enzymes, and low platelets. Requires urgent care.
Platelet Disorders
Lipoprotein(a): The Silent Heart Risk You Need to Know
Lp(a): genetic risk for clots & heart disease. Not lowered by diet. Tests measure levels. Manage other risk factors.
Pulmonary Embolism (PE)
A pulmonary embolism (PE) is a life-threatening blockage in lung arteries, often from a leg clot. Urgent diagnosis and treatment are vital.
HELLP Syndrome
HELLP syndrome: A serious pregnancy issue with hemolysis, elevated liver enzymes, and low platelets. Requires urgent care.
Lipoprotein(a): The Silent Heart Risk You Need to Know
Lp(a): genetic risk for clots & heart disease. Not lowered by diet. Tests measure levels. Manage other risk factors.
Heparin-Induced Thrombocytopenia
Heparin-induced thrombocytopenia (HIT) is a rare but serious reaction to heparin. It causes low platelet counts & raises clotting risk. Early diagnosis and stopping heparin are crucial.
Peripheral Artery Disease (PAD)
PAD: Narrowed leg arteries causing pain, slow healing. Risk factors include smoking & diabetes. Early detection is key to prevent complications.
Heparin-Induced Thrombocytopenia
Heparin-induced thrombocytopenia (HIT) is a rare but serious reaction to heparin. It causes low platelet counts & raises clotting risk. Early diagnosis and stopping heparin are crucial.
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.
Catastrophic Antiphospholipid Syndrome
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
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)
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder causing abnormal blood vessels, leading to frequent nosebleeds and internal bleeding.