At least 50% of individuals with WM have hyperviscosity syndrome, an increased viscosity or thickening of the blood caused by the accumulation of IgM in the serum.
Waldenstrom's macroglobulinemia is not considered hereditary, as most cases occur sporadically without a clear genetic link. However, some studies suggest a potential association with certain genetic predispositions, particularly in families with other lymphoproliferative disorders. While having a family history of related conditions may slightly increase risk, the majority of patients do not have a direct hereditary connection. Always consult a healthcare professional for personalized information regarding risk factors.
Many individuals with WM have no symptoms of the disease. This is known as asymptomatic macroglobulinemia. When symptoms of WM are present, they may vary greatly
No. Diabetes is when your blood sugar is low. Anemia is when your deprived of iron in your diet.
Folic acid deficiency anemia
There is no known prevention for WM
No. They are not related.
iron
It was first identified in 1944, by the Swedish physician Jan Gosta Waldenstrom
Radiation-induced anemia is typically due to damage to the bone marrow, resulting in a decrease in red blood cell production. This type of anemia is called aplastic anemia, where the bone marrow fails to produce enough blood cells.
not sure
There also is no generally-accepted course of treatment for WM.
i dont know thats why i am asking you