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Hereditary spherocytosis is an inherited blood disorder. It happens because of a problem with the red blood cells (RBCs). Instead of being shaped like a disk, the cells are round like a sphere.
These red blood cells (called spherocytes) are more fragile than disk-shaped RBCs. They break down faster and more easily than normal RBCs. This breakdown leads to anemia (not enough RBCs in the body) and other medical problems. Anemia caused by breaking down of RBCs is called hemolytic anemia.
Symptoms may range from mild to severe. Treatments can help with symptoms.
Symptoms of hereditary spherocytosis (sfir-oh-sye-TOE-sis) can vary and start at any age. Most people with the condition have a mild to moderate anemia. Anemia can cause:
When RBCs break down, they release a colored substance called bilirubin. Many RBCs break down in hereditary spherocytosis, so there's more bilirubin in the body than normal. The higher level of bilirubin can lead to:
Some people also might have:
People usually inherit hereditary spherocytosis from their parents. Talking to a genetic counselor can help someone with the condition understand how it runs in families.
If someone has symptoms of hereditary spherocytosis, such as anemia, doctors will look for the cause. They will:
Treatment for hereditary spherocytosis depends on the symptoms. Some people never need treatment.
When treatments are done, they may include:
Babies with severe symptoms may need:
These treatments don't cure the condition, but they do manage symptoms.
Some infections can be very serious in young children whose spleen was removed. So they'll need certain vaccines (shots) and special care if they get a fever.
Some children with hereditary spherocytosis don't need any medical treatments. If treatment is needed, help your child get the best care:
Note: All information is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.
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