Factor V Leiden: A Comprehensive Guide to the Genetic Clotting Disorder
Introduction & Background of Factor V Leiden Factor V Leiden is the most common inherited form of thrombophilia, a condition […]
Introduction & Background of Factor V Leiden Factor V Leiden is the most common inherited form of thrombophilia, a condition […]
Introduction & Background of Brugada Syndrome Brugada Syndrome (BrS) is a rare but potentially life-threatening genetic heart rhythm disorder (arrhythmia). […]
Introduction & Background of Erythromelalgia Erythromelalgia (EM), often called “Man on Fire Syndrome,” is a rare and complex neurological disorder […]
Introduction & Background of Thrombotic Thrombocytopenic Purpura (TTP) Thrombotic Thrombocytopenic Purpura (TTP) is a rare, life-threatening blood disorder characterized by […]
Introduction & Background of Cryoglobulinemia Cryoglobulinemia is a rare medical condition characterized by the presence of abnormal proteins in the […]
Introduction & Background of Brugada Syndrome Brugada Syndrome (BrS) is a rare but potentially life-threatening genetic heart rhythm disorder (arrhythmia). […]
Introduction & Background of Paroxysmal Nocturnal Hemoglobinuria (PNH) – Red Blood Cell Destruction Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare, […]
Introduction & Background of Dermatomyositis Dermatomyositis (DM) is a rare inflammatory disease that is classified as an idiopathic inflammatory myopathy. […]
Introduction & Background of Hashimoto’s Encephalopathy – Brain dysfunction linked to autoimmune thyroiditis Hashimoto’s Encephalopathy (HE) is a rare and […]
Introduction & Background of Anti-NMDA Receptor Encephalitis Anti-NMDA Receptor Encephalitis is a severe form of autoimmune encephalitis (brain inflammation) where […]