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Sickle Cell Disease: Information for Parents

Sickle Cell Disease Information for Parents Sickle Cell Disease Information for Parents

Every year, roughly 2,000 babies are born with sickle cell disease, the most common inherited blood disorder in the United States. Children with sickle cell disease experience episodes of severe pain and ongoing medical challenges. Early and ongoing medical care can minimize complications and help children with the disorder lead full and active lives.

In children with sickle cell disease, a protein called hemoglobin inside the red blood cells forms chains that clump together and cause the red blood cell to be shaped like a crescent moon or the letter C―called a sickle cell.

Compared to normal red blood cells that are disk-shaped and flexible, sickled cells are stiff, sticky and fragile. They break apart and leave the blood stream sooner than normal red blood cells. This results in blocking of normal blood flow, preventing blood, and the oxygen it carries, to get to everywhere in the body.


Image Source: U.S. National Library of Medicine

How do infants and children get sickle cell disease?

Babies are born with sickle cell disease. Sickle cell disease is a genetic condition, so children get it in the same way they inherit the color of their eyes, skin, and hair through the combination of genes they inherit from their parents.

How is sickle cell disease inherited?

Everyone inherits one hemoglobin gene from their mother and one hemoglobin gene from their father. Inheriting one mutated or abnormal gene, but having a normal gene from the other parent, is called having a trait. Inheriting two abnormal hemoglobin traits or genes determines whether a child has sickle cell disease.

The normal hemoglobin gene is labeled A. The most common mutated hemoglobin genes or hemoglobin traits are called S or C. The mutated (changed) hemoglobin gene associated with sickle cell disease is S. Common types of mutated (changed or abnormal) hemoglobin genes that combine with S to cause sickle cell disease are S, C and Beta thalassemia.

People who have inherited one of the following gene combinations DO NOT have sickle cell disease:

  • A + A (AA): no sickle cell disease

  • A + S (AS): carrier of the hemoglobin "S" gene, known as sickle cell trait

  • A + C (AC): carrier of the hemoglobin "C" gene

People who have inherited one of the following gene combinations DOhave sickle cell disease:

  • S + S (SS): Sickle cell anemia or Hemoglobin SS

  • S + C (SC): Sickle hemoglobin C disease or Hemoglobin SC

  • S + beta thalassemia trait (S-beta thalassemia): a form of sickle cell disease

Image source: Centers for Disease Control and Prevention

How do I know if my baby has sickle cell trait or disease?

Every state in the US performs a newborn screening test for sickle cell disease. If this test is concerning for sickle cell disease, the baby is referred to a pediatric hematologist. If the test indicates sickle cell trait, the parents are counselled by the general pediatrician and the child generally does not need to see a hematology specialist.

Early diagnosis, before infants show any symptoms allows infants with sickle cell disease to get early treatment and may decrease their risk of infections or other serious complications.

Why is sickle cell disease more common in children of African heritage?

A carrier of a single hemoglobin S gene is said to have sickle cell trait or hemoglobin S trait. About 1 in 12 people of African ancestry carry S trait. Sickle cell trait is also common in people with ancestors from the Caribbean, Middle East, India, South America, Central America and Mediterranean countries such as Turkey, Greece and Italy. Sickle cell trait is found today in descendants of these populations no matter where they live.

People with hemoglobin S trait alone do NOT have sickle cell disease. However, if their reproductive partner also has the hemoglobin S trait, then together they have a 1 in 4 chance (25%) of having a child with sickle cell disease. This is why even bi-racial and/or multi-racial children can have sickle cell disease; About 1 in 365 people of African ancestry have sickle cell disease.

Why is sickle cell disease sometimes called sickle cell anemia?

Sickle cell disease is an umbrella term for the many specific types of sickle cell disorders. Anemia―meaning a lower-than-normal number of red blood cells―happens with all forms of sickle cell disease. While normal red blood cells can live for 120 days, sickled cells last only 7 to 20 days; the body can't replace them fast enough resulting in anemia.

Children who have inherited two abnormal genes have sickle cell disease; which specific genes have been inherited determines what the disorder is called. Sickle cell anemia refers to the two most severe forms of sickle cell disease, hemoglobin SS and sickle beta zero thalassemia.

Main Types of Sickle Cell Disorders

Hemoglobin SS

The most severe form, affecting 65% of children with sickle cell disease. Most or all of the hemoglobin is abnormal, causing chronic anemia.

Hemoglobin SC disease

Roughly 25% of children with sickle cell disease have this mild to moderate form of the disease. Symptoms generally develop later in childhood, but may be as severe as in SS.

Sickle beta plus thalassemia

Affects around 8% of children with sickle cell disease. This is generally considered a mild form of sickle cell disease, but severity can vary greatly.

Sickle beta zero thalassemia

A severe but less common form, accounting for 2% of sickle cell disease. It is similar to hemoglobin SS.


Why are infants and children with sickle cell disease at higher risk of infection?

Sickle cell disease may cause damage to the spleen, kidneys, lungs and brain. Once damaged by sickled cells the spleen may not be able to filter bacteria from the blood as well as it normal.

As a result, infants and children with sickle cell disease have a compromised immune system, which means they are more likely to have certain infections which may be fatal.

Antibiotics to prevent secondary infections in infants & children with sickle cell disease:

National guidelines recommend newborns diagnosed with severe sickle cell disease (SS and S beta zero thalassemia) receive antibiotics twice a day until they are 5 years old.

Research shows that children with sickle cell anemia given twice daily penicillin (an antibiotic) had 84% less risk of Streptococcus pneumoniae bacterial infection, which can cause serious conditions like pneumonia and meningitis.

What is outlook for children with sickle cell disease?

Sickle cell disease is a chronic disease, but the outlook is improving. Early diagnosis and starting antibiotics shortly after birth for those with severe forms of sickle cell have greatly improved life expectancy. Today other treatments are available to minimize complications which can improve quality of life and life expectancy.

Is there a cure for sickle cell disease?

Stem cell (bone marrow) transplants is the only cure for sickle cell disease. This treatment requires a donor with suitable bone marrow. Similar to other treatments stem cell transplant has benefits and risks which should be discussed before proceeding. Other promising treatments being explored include gene therapy. A collaborative research effort led by the U.S. National Heart, Lung, and Blood Institute was created in 2018 to speed up the search for cures.

Who are the doctors that care for children with sickle cell disease?

In addition to regular visits with their pediatrician, children with sickle cell disease should see a pediatric hematologist at least periodically. These doctors specialize in the care of children with sickle cell disease.

More information:

Last Updated
9/2/2022
Source
American Academy of Pediatrics Section on Hematology/Oncology (Copyright © 2022)
The information contained on this Web site should not be used as a substitute for the medical care and advice of your pediatrician. There may be variations in treatment that your pediatrician may recommend based on individual facts and circumstances.
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