Thalassemia: An inherited defect in the ability to produce hemoglobin, usually seen in persons of Mediterranean background.
Thalassemia
Thalassemia
Inherited hemolytic anemias are caused by inborn defects in components of the red blood cells--the cell membrane, the enzymes, or the hemoglobin
An inherited disorder that interferes with the normal production of hemoglobin
iron deficiency anemia, thalassemia (an inherited disease in which globin chain production is deficient), and anemias associated with chronic infection or disease.
Infertility
there is an inability for Oxygen to properly bond to the Hemoglobin molecules in the damaged cell
The inability to produce insulin is the cause of type I diabetes mellitus. Not being able to use insulin effectively causes Type II diabetes mellitus.
The inability to produce insulin is the cause of type I Diabetes mellitus. Not being able to use insulin effectively causes Type II diabetes mellitus.
Diabetes mellitus
Fetal hemoglobin (Hemoglobin F), Alkali-resistant hemoglobin, HBF (or Hb F), is the major hemoglobin component in the bloodstream of the fetus. After birth, it decreases rapidly until only traces are found in normal.
There are two categories of hemoglobinopathy. In the first category, abnormal globin chains give rise to abnormal hemoglobin molecules. In the second category, normal hemoglobin chains are produced but in abnormal amounts.