Platelet function disorders disrupt blood clotting, causing excessive bleeding. Inherited or acquired, these conditions can range from mild to severe.
Platelet Disorders
Thrombocytopenia
Thrombocytopenia, a condition with a low platelet count, can cause easy bruising and bleeding. While it often has no symptoms, severe cases can lead to internal bleeding. It can arise from various causes, including infections, medications, or autoimmune disorders. Early diagnosis and treatment are crucial to prevent complications.
Vascular Bleeding Disorders
Vascular bleeding disorders come in two forms: inherited (passed down in families) and acquired (developed throughout life due to factors like vitamin deficiencies or medications). Both cause easy bruising & abnormal bleeding.
Hereditary Hemorrhagic Telangiectasia (HHT)
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder causing abnormal blood vessels, leading to frequent nosebleeds and internal bleeding.
Ehlers-Danlos Syndrome (EDS)
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.
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.
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.