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There are many kinds of diseases that affect your red blood cells and Hereditary Spherocytosis is just one of them. It is defined as an acute autosomal abnormality of erythrocytes, which is rather dominant. The most common symptoms of this problem includes anemia, lack of red blood cells in the body, broken down cell and iron deficiency.
HOW IS HEREDITARY SPHEROCYTOSIS DIAGNOSED?
Essentially, Hereditary Spherocytosis speeds up the process of breaking down the red blood cells faster than the healthy ones and as a result, the body will produce too much bilirubin in the bloodstream.
HOW IS HEREDITARY SPHEROCYTOSIS TREATED?
Though the severity of the disorder will determine the treatment for Hereditary Spherocytosis, doctors prefer to surgically remove the spleen to treat the condition. This procedure, known as splenectomy and by removing the spleen, the problem of the red blood cells dying can be prevented thereby improving their life. In the case of children and other milder forms of the condition, other treatments, including oral medication may be adopted.
DID YOU KNOW?
Hereditary Spherocytosis can actually lead to severe conditions like jaundice and gallstones.