FirstHope

Hemophilia Introduction Hemophilia is an inherited bleeding disorder characterized by a deficiency in specific clotting factors, leading to prolonged bleeding. The two most common types are Haemophilia A and Haemophilia B. Types Hemophilia A Deficiency: Clotting factor VIII. Genetics: X-linked recessive inheritance, primarily affecting males. Hemophilia B Deficiency: Clotting factor IX. Genetics: X-linked recessive inheritance, … Read more

Hereditary anemia is caused by genetic mutations that affect the production, structure, or function of RBCs. Common Types of Hereditary Anemia: Sickle Cell Anemia Mutation in the HBB gene leads to abnormal hemoglobin S (HbS). Thalassemia Mutations in genes producing alpha or beta globin chains. Hereditary Spherocytosis Mutations in genes encoding RBC membrane proteins, causing … Read more

Thalassemia Introduction Thalassemia is a group of inherited blood disorders caused by mutations affecting hemoglobin production. Results in reduced production of either alpha or beta globin chains, leading to imbalanced globin synthesis, ineffective erythropoiesis, and hemolysis. Categorized into alpha and beta thalassemia based on the affected globin chain. Types of Thalassemia Alpha  Caused by deletions or … Read more

Acquired anemias result from external factors or conditions that affect RBC production or lifespan. Common Types Acquired Anemia Iron Deficiency Anemia Due to inadequate iron intake, absorption issues, or chronic blood loss. Vitamin B12 and Folate Deficiency Anemia Caused by poor dietary intake, malabsorption, or increased demand. Anemia of Chronic Disease Associated with chronic infections, … Read more

Iron Deficiency Anemia Introduction Iron Deficiency Anemia occurs  the body lacks enough iron to produce hemoglobin, the protein in red blood cells (RBCs) that carries oxygen from the lungs to the rest of the body. Iron is a critical component of hemoglobin, and its deficiency leads to reduced RBC production and anemia. Causes of Iron … Read more

Megaloblastic Anemia Introduction Megaloblastic anemia is a type of anemia characterized by the presence of large, abnormal red blood cells (megaloblasts) in the bone marrow and peripheral blood. It is primarily caused by deficiencies in vitamin B12 or folic acid, both essential for DNA synthesis. Causes of Megaloblastic Anemia: Vitamin B12 Deficiency Dietary Deficiency: Insufficient … Read more

Sickle Cell Anemia Introduction Sickle cell anemia is a genetic disorder caused by a mutation in the HBB gene, which encodes the beta-globin subunit of hemoglobin. This mutation leads to the production of abnormal hemoglobin known as hemoglobin S (HbS). Under low oxygen conditions, HbS polymerizes, causing red blood cells (RBCs) to become rigid and … Read more

Epilepsy is a chronic neurological disorder characterized by recurrent, unprovoked seizures due to abnormal electrical activity in the brain. Seizures can vary in type and severity, ranging from brief lapses in attention or muscle jerks to severe and prolonged convulsions. Causes of Epilepsy Genetic Factors: Certain types of epilepsy are linked to genetic mutations. Structural … Read more

Chronic renal failure, also known as chronic kidney disease (CKD), is a gradual and progressive decline in kidney function that occurs over months to years. CKD can eventually lead to end-stage renal disease (ESRD), in which the kidneys are no longer able to function adequately to maintain the body’s homeostasis. ESRD requires renal replacement therapy, … Read more

Acute renal failure, also known as acute kidney injury (AKI), is a sudden and rapid decline in kidney function that occurs over a short period, usually within hours to days. It can result in the buildup of waste products, electrolyte imbalances, and fluid retention in the body, which can be life-threatening if not promptly treated. … Read more