Sickle Cell Disease in Children
What is sickle cell disease in children?
Sickle cell disease (SCD) is a
blood disorder that a child is born with. It's passed down through a parent’s genes.
Children with SCD make an abnormal type of hemoglobin. This is the protein in red blood
cells that carries oxygen to all parts of the body. With SCD, the body organs and
tissues don’t get enough oxygen.
Healthy red blood cells with normal
hemoglobin are round and move easily through blood vessels. When a child has SCD, the
red blood cells are hard and sticky. They are shaped like the letter C (and like a farm
tool called a sickle). These damaged red blood cells (sickle cells) clump together. They
can’t move easily through the blood vessels. They get stuck in small blood vessels and
block blood flow. This blockage can cause pain. It can also damage major organs.
Sickle cells die sooner than healthy cells. Normally the spleen helps filter infections out of the blood. But sickle cells get stuck in this filter and die. Having fewer healthy red blood cells causes anemia. The sickle cells can also damage the spleen. Without a healthy spleen, children are more at risk for serious infections.
There are several complex types of the sickle cell gene. Some don’t cause symptoms or severe problems, but others do. Talk to your child’s healthcare provider about the specific form of sickle cell your child has.
Most children with SCD will start showing symptoms during the first year, often around 5 months.
What causes sickle cell disease in a child?
Sickle cell is present at birth. It
is inherited when a child has 2 sickle cell genes, 1 from each parent.
A child who has only one sickle cell gene is healthy. But he or she is a carrier of the disease. If two carriers have a child, there is a greater chance their child will have sickle cell disease.
Once parents have had a child with
sickle cell disease, there is a 1 in 4 chance that another child will be born with
sickle cell disease. There is also a 1 in 2 chance that a child will be a carrier, like
Which children are at risk for sickle cell disease?
Having a family history of SCD
increases a child’s risk for the disease. SCD mainly affects people whose families came
from Africa, and Hispanics whose families are from the Caribbean. But the gene has also
been found in people whose families are from the Middle East, India, Latin America, and
Mediterranean countries. It has also been found in American Indians.
What are the symptoms of sickle cell disease in a child?
Most children with SCD will start to have symptoms during the first year of life, often around 5 months. Each child’s symptoms may vary. They may be mild or severe. Symptoms can include:
- Anemia. This is the most common symptom. Having fewer red blood cells causes anemia. Anemia can make a child pale and tired.
- Yellowing of the skin, eyes, and mouth
(jaundice). This is a common symptom. Sickle cells don't live as long as
normal red blood cells. They die faster than the liver can filter them out. The
yellow color is caused by a substance (bilirubin) that is released when the red blood
- Pain crisis, or sickle crisis. When sickle cells move through small blood vessels, they can get stuck. This blocks blood flow and causes pain. This sudden pain can happen anywhere, but most often occurs in the chest, arms, and legs. Babies and young children may have painful finger and toe swelling. Blocked blood flow may also cause tissue death.
- Acute chest syndrome. This is when sickle cells stick together and block oxygen flow in the tiny vessels in the lungs. This can be deadly. It often occurs suddenly, when the body is under stress from infection, fever, or fluid loss (dehydration). It looks like pneumonia and can include fever, pain, and a violent cough.
- Splenic sequestration (pooling). The spleen becomes enlarged and painful when sickle cells get stuck and build up there. Fewer red blood cells are able to move. This can cause a sudden drop in hemoglobin. It can be deadly if not treated at once.
The symptoms of SCD may look like other disorders or health problems. Always see your child's healthcare provider for a diagnosis.
How is sickle cell disease diagnosed in a child?
Most states check newborn babies for abnormal hemoglobin as part of routine newborn screening tests. State newborn screening includes tests for all newborns within the first few days of life. These tests identify serious, life-threatening diseases.
SCD may be found as part of newborn screening. Your family history, your child's medical history, and a physical exam are all included in the diagnosis. If the screening test shows SCD, a blood test called hemoglobin electrophoresis may be done. It can tell if your child is a carrier of sickle cell. It can also tell if your child has any of the diseases linked to the sickle cell gene. Other blood tests may also be done.
How is sickle cell disease treated in a child?
Treatment will depend on your child’s symptoms, age, and general
health. It will also depend on how severe the condition is.
Early diagnosis and preventing
further problems is important in treating this disease. Your child's healthcare provider
will refer you to a hematologist. This is an expert in blood disorders. Other
specialists may also be involved in your child's care.
Treatment may include:
- Pain medicines. These are used for
- Drinking plenty of water daily (8 to 10
glasses). This helps prevent and treat pain crises. In some cases, IV
(intravenous) fluids may be needed.
- Blood transfusions. These are used to
treat anemia, chronic pain, acute chest syndrome, and splenic sequestration, and to
- Vaccines and antibiotics.
These are used to prevent infections.
- Folic acid. This helps prevent severe
- Regular eye exams. These are done to
screen for an eye condition called retinopathy. Have your child’s eyes checked each
- Stem cell transplant. Transplants can
cure some children with SCD. Studies of this treatment are ongoing. Talk with your
child’s healthcare provider. Transplants are only done at certain medical
- Hydroxyurea. This is a medicine that can reduce the
number of sickle cells in the blood. It reduces complications, painful episodes
(crises), and hospital stays.
What are the possible complications of sickle cell disease in a child?
Complications of SCD include:
- Long-term anemia. This may lead to
delayed healing and delayed growth and development.
- Pain crisis, or sickle crisis. In
severe cases, your child may need treatment in a hospital.
- Acute chest syndrome. Over time, many
episodes of acute chest syndrome can cause lasting (permanent) lung damage
- Splenic sequestration (pooling). When
red blood cells build up in the spleen, it becomes enlarged and painful. The spleen
can be damaged and scarred after many episodes of splenic sequestration. By age 8,
many children with SCD have had their spleen removed. Or they may have lasting damage
from repeated splenic sequestration. The risk for infection is a major concern for
children without a working spleen. Infection is the major cause of death in children
younger than age 5.
- Stroke. If the blood vessels to the brain are blocked, a
stroke can occur. Serious long-term problems may result. A child who has had a stroke
is more likely to have another one.
- Infections. Babies and children with
SCD have a higher risk for infections.
- Priapism. The sickle cells block the blood vessels in the penis, causing great pain. If not treated right away, this can lead to the inability to have an erection (impotence).
SCD can affect any major organ. This can cause:
- Frequent infections
- Leg ulcers or serious sores
- Bone damage
- Kidney damage
- Eye damage
- Multiple organ failure
How can I help my child live with sickle cell disease?
Advances in preventive care and new
medicines have reduced the life-threatening problems of sickle cell. But it is still a
severe, chronic, and sometimes fatal disease. Your child should be carefully managed by
specialists. How your child is managed depends on:
- The type of sickle cell your child has
- How severe the disease is
- How often your child has complications
- How well you and your child follow preventive efforts
You may not be able to fully prevent your child from having complications of SCD. But helping your child live a healthy lifestyle can reduce some of the problems. Make sure your child has regular eye exams and gets stroke screening tests. Also talk with your child’s healthcare provider about making sure your child:
- Eats a healthy diet
- Gets enough sleep
- Drinks plenty of fluids
Stay away from things that may
trigger a crisis for your child. These include:
- High altitudes
- Cold weather
- Swimming in cold water
Help your child prevent infections
- Staying away from people who are sick
- Washing his or her hands often
- Having all recommended vaccines such
- Having all recommended screenings such
as hepatitis C
When should I call my child's healthcare provider?
Call your child's healthcare provider or get medical care right away if your child has:
- Sudden pain, mainly in the chest, belly, arms, or legs
- Symptoms of an enlarged spleen
- Trouble breathing
- Sudden loss of vision
- Symptoms of severe anemia
Key points about sickle cell disease in children
- Sickle cell disease (SCD) is an inherited blood disorder that is present at birth. This means it is passed down through a parent’s genes.
- With SCD, the red blood cells have an abnormal C shape. They get stuck in small blood vessels and block blood flow.
- This blockage can cause pain and lead to infection. It can also damage a child’s major organs, and cause a stroke.
- Newborns are checked for sickle cell disease as part of a group of screening tests.
- Most children will start to have symptoms during the first year of life, often around 5 months.
Tips to help you get the most from a visit to your child’s healthcare provider:
Online Medical Reviewer:
L Renee Watson MSN RN
Online Medical Reviewer:
Richard LoCicero MD
Date Last Reviewed:
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