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.
Platelet Disorders
Embolus & Embolism
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.
Tissue Plasminogen Activator (tPA)
tPA is a powerful drug used to dissolve blood clots causing heart attacks, strokes, and pulmonary embolisms. While effective, it also carries risks, primarily bleeding.
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.
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.
Prothrombin Time (PT) & INR
The PT assay is used to diagnose and monitor a variety of bleeding and clotting disorders by measuring how long it takes a blood clot to form.
Immune Thrombocytopenia (ITP)
Immune thrombocytopenia (ITP) is a rare autoimmune disorder in which the body’s immune system destroys its own platelets.
Disseminated Intravascular Coagulation (DIC)
Disseminated intravascular coagulation (DIC) occurs when the blood coagulation system is overwhelmed causing widespread blood clots and bleeding throughout the body.
Hemophilia
Hemophilia is a rare inherited blood disorder that affects the ability of blood to clot. People with hemophilia often bleed for longer than usual after an injury or surgery.
Hemorrhagic Disease of the Newborn
Hemorrhagic disease of the newborn is a bleeding disorder that occurs in newborns due to a deficiency of vitamin K.
von Willebrand Disorder (vWD)
Von Willebrand disorder (VWD) is a common inherited bleeding disorder caused by a deficiency of von Willebrand factor (vWF), a protein that helps blood clot.