Hereditary Spherocytosis Treatment

Hereditary spherocytosis is a genetic condition that causes red blood cells to be shaped like spheres instead of discs. This makes the cells break down more quickly, resulting in anemia (a reduced red blood cell count). Symptoms may include feeling tired, pale skin, and jaundice (yellowing of the skin or eyes).

Hereditary spherocytosis is usually passed down in families. This means a child can inherit it from a parent through a gene change. Sometimes, a child may be the first in the family to have the condition. They could pass it on to their children.

Find out more about hereditary spherocytosis on the Together by St. Jude™ online resource.

Hereditary spherocytosis treatment

Some people with hereditary spherocytosis have mild or no symptoms.  

People with mild symptoms may not need treatment. For others who have more symptoms, treatment may be needed to manage complications. Treatments for hereditary spherocytosis may include blood transfusions and surgery.

Hereditary spherocytosis clinical trials

St. Jude offers clinical trials and research studies for children, teens, and young adults with hereditary spherocytosis.

Learn more about clinical research at St. Jude.

Hereditary spherocytosis care at St. Jude

St. Jude provides the highest quality of care for patients with hereditary spherocytosis:

• At St. Jude, we have created an environment where children can be children and families can be together. 
• The nurse-to-patient ratio at St. Jude is about 1:3 in hematology and oncology and 1:1 in the Intensive Care Unit.  
• We offer a dedicated team of specialists to meet the needs of children with hereditary spherocytosis, including:  
  • Surgeons, doctors, advanced practice providers, and nurses who treat this disorder 
  • Genetic counselors 
  • Clinical dietitians 
  • Child life specialists 
  • Psychologists 
  • Researchers and scientists 
• Patients may be able to get expert, compassionate care and treatment closer to their homes through the St. Jude Affiliate Program. 

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