Glycogen Storage Disease in Children
What is glycogen storage disease?
Glycogen storage disease (GSD) is a rare condition that changes the way the body uses
and stores glycogen, a form of sugar or glucose.
Glycogen is a main source of energy for the body. Glycogen is stored in the liver.
When the body needs more energy, certain proteins called enzymes break down glycogen
into glucose. They send the glucose out into the body.
When someone has GSD, they are missing one of the enzymes that breaks down glycogen.
When an enzyme is missing, glycogen can build up in the liver. Or glycogen may not
form properly. This can cause problems in the liver or muscles, or other parts of
GSD is passed down from parents to children (is hereditary). It is most often seen
in babies or young children. But some forms of GSD may appear in adults.
Types of GSD
Experts know of at least 9 types of GSD. They are grouped by the enzyme that is missing
in each one. Each GSD has its own symptoms and needs different treatment.
The most common types of GSD are types I, III, and IV:
- Type I or von Gierke’s disease. This is the most common form of GSD. People with type I don’t have the enzyme needed
to turn glycogen into glucose in the liver. Glycogen builds up in the liver. Symptoms
often appear in babies around 3 to 4 months old. They may include low blood sugar
(hypoglycemia) and a swollen belly because of an enlarged liver.
- Type III or Cori’s disease. People with type III don’t have enough of an enzyme (the debranching enzyme) that
helps break down glycogen. The glycogen can’t fully break down. It collects in the
liver and in muscle tissues. Symptoms include a swollen belly, delayed growth, and
- Type IV or Anderson’s disease. People with type IV form abnormal glycogen. Experts think the abnormal glycogen triggers
the body’s infection-fighting system (immune system). This creates scarring (cirrhosis)
of the liver and other organs such as muscle and the heart.
What causes glycogen storage disease?
Glycogen storage disease is passed down from parents to children (hereditary).
It happens because both parents have an abnormal gene (gene mutation) that affects
a specific way that glycogen is stored or used. Most GSDs occur because both parents
pass on the same abnormal gene to their children.
In most cases parents don’t show any symptoms of the disease.
Who is at risk for glycogen storage disease?
Glycogen storage disease is passed down from parents to children (inherited). Someone
is more at risk for GSD if they have a family member with the disease.
What are the symptoms of glycogen storage disease?
With many types of GSD, symptoms first appear in babies or in very young children.
Symptoms will vary based on the type of GSD a child has, and on which enzyme he or
she is missing.
Because GSD most often affects the muscles and the liver, those areas show the most
General symptoms of GSD may include:
- Not growing fast enough
- Not feeling comfortable in hot weather (heat intolerance)
- Bruising too easily
- Low blood sugar (hypoglycemia)
- An enlarged liver
- A swollen belly
- Weak muscles (low muscle tone)
- Muscle pain and cramping during exercise
Symptoms for babies may include:
- Too much acid in the blood (acidosis)
- High blood cholesterol levels (hyperlipidemia)
The symptoms of GSD may look like other health problems. Always see your child’s healthcare
provider to be sure.
Some types of GSD can appear in adults. See your healthcare provider if you think
you may have GSD.
How is glycogen storage disease diagnosed?
Your child’s healthcare provider will ask about your child’s symptoms and past health.
The provider will do a physical exam to check for symptoms such as an enlarged liver
or weak muscles.
Your child’s provider may do a few blood tests. He or she may also take a small tissue
sample (biopsy) of your child’s liver or muscle. The sample will be taken to a lab.
It will be tested to see how much of a certain enzyme is in that part of the body.
If you are pregnant and concerned about GSD, your healthcare provider may do some
tests before your baby is born (prenatal tests) to check for GSD.
How is glycogen storage disease treated?
Treatment will vary depending on what type of GSD your child has.
For types I, III, and IV, your child’s healthcare provider may suggest a special diet
to help control symptoms. Your child may also have to take certain medicines.
For other types of GSD, your child may need to limit exercise to avoid muscle cramps.
He or she may need to have a medical treatment to replace the enzyme that is missing
(enzyme replacement therapy).
What are the complications of glycogen storage disease?
Glycogen buildup can hurt the liver and muscles. This can create other problems if
your child has certain types of GSD such as:
- Type III. This can cause harmless (benign) tumors in the liver.
- Type IV. Over time this can cause scarring (cirrhosis) of the liver. This disease leads to
Can glycogen storage disease be prevented?
There is no way to prevent glycogen storage disease. But early treatment can help
control symptoms once a child has GSD.
If you or your partner have GSD, or a family history of this disease, see a genetic
counselor before you get pregnant. He or she can find out your chances of having a
child with GSD.
Living with glycogen storage disease
A child with GSD may have special needs. Be sure that your child gets regular medical
care. It is important that his or her healthcare provider checks your child’s condition.
Regular medical visits will also help you keep up with new treatment options.
Online or in-person support groups may also be helpful for you and your family.
When should I call my child’s healthcare provider?
Many forms of glycogen storage disease appear in babies and young children.
Call your healthcare provider if your baby’s behavior changes after you stop night
Talk with your healthcare provider if your child:
- Is not growing fast enough
- Has constant (chronic) hunger
- Has a swollen belly
Teens and adults should watch for the following symptoms when they exercise:
- Muscle weakness
- Glycogen storage disease (GSD) is a rare condition that changes the way the body uses
and stores glycogen, a form of sugar.
- It is passed down from parents to children (inherited). For most GSDs, each parent
must pass on one abnormal copy of the same gene.
- Most parents do not show any signs of GSD.
- There are at least 9 known types of GSD. Each GSD has its own symptoms and needs different
- Symptoms often first appear in babies or young children. In some cases GSD can appear
Tips to help you get the most from a visit to your child’s healthcare provider:
- Know the reason for the visit and what you want to happen.
- Before your visit, write down questions you want answered.
- At the visit, write down the name of a new diagnosis, and any new medicines, treatments,
or tests. Also write down any new instructions your provider gives you for your child.
- Know why a new medicine or treatment is prescribed and how it will help your child.
Also know what the side effects are.
- Ask if your child’s condition can be treated in other ways.
- Know why a test or procedure is recommended and what the results could mean.
- Know what to expect if your child does not take the medicine or have the test or procedure.
- If your child has a follow-up appointment, write down the date, time, and purpose
for that visit.
- Know how you can contact your child’s provider after office hours. This is important
if your child becomes ill and you have questions or need advice.