What is Hereditary spherocytosis?
Hereditary spherocytosis (HS) is a disorder of the surface, called the membrane, of your red blood cells. It causes your red blood cells to be shaped like spheres instead of flattened discs that curve inward. The spherical cells are less flexible than normal red blood cells.
In a healthy body, the spleen starts the immune system’s response to infections. The spleen filters bacteria and damaged cells out of the blood stream. However, spherocytosis makes it difficult for red blood cells to pass through your spleen due to the cells’ shape and stiffness.
The irregular shape of the red blood cells can cause the spleen to break them down faster. This breakdown process is called hemolytic anemia. A normal red blood cell can live for up to 120 days, but red blood cell with hereditary spherocytosis might live for as few as 10 to 30 days.
How common is Hereditary spherocytosis?
People of any race can have hereditary spherocytosis, but it’s most common in people of Northern European descent. Please discuss with your doctor for further information.
What are the symptoms of Hereditary spherocytosis?
Hereditary spherocytosis can range from mild to severe. Symptoms vary depending on the severity of the disease. Most individuals with HS have moderate disease. People with mild HS may be unaware they have the disease.
Common signs and symptoms of Hereditary spherocytosis are:
Spherocytosis causes your red blood cells to break down faster than healthy cells do, which can lead to anemia. If spherocytosis causes anemia, you may appear paler than normal. Other common symptoms of anemia from hereditary spherocytosis can include:
- Shortness of breath
- Dizziness or lightheadedness
- Increased heart rate
- Heart palpitations
When a blood cell breaks down, the pigment bilirubin is released. If your red blood cells break down too quickly, it leads to too much bilirubin in your bloodstream. An excess of bilirubin can cause jaundice. Jaundice causes the skin to turn yellowish or bronze. The whites of the eyes can also turn yellow.
Excess bilirubin can also cause gallstones, which can develop in your gallbladder when too much bilirubin gets into your bile. You may not have any symptoms of gallstones until they cause a blockage. Symptoms may include:
- Sudden pain in your upper right abdomen or below your breastbone
- Sudden pain in your right shoulder
- Decreased appetite
Symptoms in children
Infants may show slightly different signs of spherocytosis. Jaundice is the most common symptom in newborns, rather than anemia, especially in first week of life. Call your child’s pediatrician if you notice that your infant:
- Has yellowing of the eyes or skin
- Is restless or irritable
- Has difficulty feeding
- Sleeps too much
- Produces fewer than six wet diapers per day
The onset of puberty may be delayed in some children who have HS. Overall, the most common findings in hereditary spherocytosis are anemia, jaundice, and an enlarged spleen.
There may be some symptoms not listed above. If you have any concerns about a symptom, please consult your doctor.
When should I see my doctor?
If you or your loved one has any signs or symptoms listed above or you have any questions, please consult with your doctor. Everyone’s body acts differently. It is always best to discuss with your doctor what is best for your situation.
What causes Hereditary spherocytosis?
Hereditary spherocytosis is the predominant cause of spherocytosis, and is caused by several genetic mutations that lead to membrane abnormalities of red blood cells. The disease usually is inherited as an autosomal dominant trait; although a few people with hereditary spherocytosis may develop it secondary to new mutations. In addition, there is an autosomal recessive mode of inheritance that also may occur in about 20%-25% of all individuals with hereditary spherocytosis.
Spherocytosis may be present in autoimmune hemolytic anemia in which autoantibodies react with red blood cells and cause alterations in their membranes that includes lysis of red blood cells. Spherocytes may develop during this destruction of red blood cells.
What increases my risk for Hereditary spherocytosis?
Hereditary spherocytosis is caused by a genetic defect. If you have a family history of this disorder, your chances of developing it are higher than someone who does not. Please consult with your doctor for further information.
Diagnosis & treatment
The information provided is not a substitute for any medical advice. ALWAYS consult with your doctor for more information.
How is Hereditary spherocytosis diagnosed?
HS is most often diagnosed in childhood or early adulthood. In about 3 out of 4 cases, there’s a family history of the condition. Your doctor will ask you about the symptoms you have. They’ll also want to know about your family and medical history.
Your doctor will perform a physical exam. They will check for an enlarged spleen, which is usually done by palpating different regions of your abdomen.
It’s likely your doctor will also draw your blood for analysis. A complete blood count test will check all your blood cell levels and the size of your red blood cells. Other types of blood tests can also be useful. For example, viewing your blood under the microscope allows the doctor to see the shape of your cells, which can help them determine if you have the disorder.
Your doctor may also order tests that check your bilirubin levels.
How is Hereditary spherocytosis treated?
There is no cure for HS, but it can be treated. The severity of your symptoms will determine which course of treatment you receive. Options include:
Surgery: In moderate or severe disease, removing the spleen can prevent common complications that result from hereditary spherocytosis. Your red blood cells will still have their spherical shape, but they’ll live longer. Removing the spleen can also prevent gallstones.
Not everyone with this condition needs to have their spleen removed. Some mild cases can be treated without surgery. Your doctor might think less invasive measures are better suited for you. For example, surgery is not recommended for children who are younger than 5 years.
Vitamins: Folic acid, a B vitamin, is usually recommended for everyone with HS. It helps you make new red blood cells. A daily dose of oral folic acid is the main treatment option for young children and people with mild cases of HS.
Transfusion: You may need red blood cell transfusions if you have severe anemia.
Light therapy: The doctor might use light therapy, also called phototherapy, for severe jaundice in infants.
Vaccination: Getting routine and recommended vaccinations are also important to prevent complications from infections. Infections can trigger the destruction of red blood cells in people with HS.
Lifestyle changes & home remedies
What are some lifestyle changes or home remedies that can help me manage Hereditary spherocytosis?
If you have any questions, please consult with your doctor to better understand the best solution for you.
Hello Health Group does not provide medical advice, diagnosis or treatment.
Review Date: February 5, 2018 | Last Modified: February 5, 2018
Hereditary Spherocytosis https://www.healthline.com/health/congenital-spherocytic-anemia Accessed February 05, 2018
Spherocytosis (Hereditary, HS) https://www.medicinenet.com/spherocytosis_hereditary_hs/article.htm#what_are_the_signs_and_symptoms_of_spherocytosis Accessed February 05, 2018