TL;DR Alpha thalassemia is an inherited hemolytic anemia due deletions or point mutation (uncommon) of the α-globin gene leading to reduced production or absence of α-chains needed for hemoglobin. It has an autosomal recessive inheritance pattern. Genetics ▾...
Introduction HPLC, or High Performance Liquid Chromatography, is a powerful tool used to detect hemoglobinopathies. Hemoglobinopathies, a group of genetic disorders that affect the structure or production of hemoglobin, the oxygen-carrying protein in red blood cells,...
Introduction The G6PD fluorescent test is a rapid and reliable method for diagnosing G6PD deficiency. The test involves measuring the activity of G6PD in a sample of red blood cells. A low level of G6PD activity indicates a deficiency. Glucose-6-phosphate...
Introduction Overview of Anemia Anemia is a common blood disorder characterized by a deficiency of red blood cells or hemoglobin, leading to a reduced oxygen-carrying capacity of the blood. This condition can manifest in various forms and can have significant health...
Introduction What are red blood cells? A red blood cell (RBC) is also known as an erythrocyte. Red blood cells are the most common type of blood cell in the human body. They are responsible for carrying oxygen from the lungs to the tissues and carbon dioxide away from...
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