| Risk Factors
Ehlers-Danlos syndrome (EDS) is a group of inherited disorders. These disorders affect
the connective tissues. This type of tissue is found all over the body. There are at least six different varieties of EDS. They are classified by the type of tissue most affected and how it is inherited.
EDS is caused by a problem in the genetic material. It mainly affects the genes that create connective tissue.
Most types of EDS affect the production of collagen. Collagen is an important part of connective tissue. It gives the tissue strength and allows it to stretch.
Having family members with EDS increases your chance of EDS.
The symptoms of EDS can vary. Some may have mild symptoms. Other may have severe and life-changing symptoms.
The most common symptoms of EDS include problems with the joints and skin. Joints are loose and unstable which can lead to:
- Joint pain
- Flat feet
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Skin is soft, fragile, and can stretch far too easily. This can lead to problems such as:
- Easy bruising
- Minor injuries turning into gaping wounds
- Slow and poor wound healing
- Difficulty suturing skin because skin tends to tear
- Skin scarring from wounds or stretching
- Fleshy outgrowths on top of scars
- Calcified nodules under the skin
- Increased risk of surgical complications
Other symptoms depend on the type of EDS you have. EDS can cause problems with:
Eyes, such as:
- Epicanthic fold—fold of skin on either side of the nose may cover the inner corner of the eye, which is common in children with EDS
- Fragile sclera—the white outer coat of the eyeball
- Hole in the globe of the eye—rare
- Lung—due to loss of normal elastic tissue
- Bones and muscles—such as chronic pain
Blood vessels—weak tissue can lead to
and rupture of blood vessels
- Blood clotting—can lead to easy bruising and bleeding
Heart valves—such as
mitral valve prolapse
- Gums—bleeding and diseases
Gastrointestinal system, such as:
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Pregnancy, such as:
- Premature birth
- Early rupture of membranes
- Bleeding during pregnancy and excessive bleeding during or after childbirth
- Uterine rupture
- Higher complications from procedures
- Muscles—low muscle tone with delayed motor development
The doctor will ask about your symptoms and medical history. A physical exam will be done. This is usually enough to diagnosis EDS in most people. When the diagnosis is uncertain, tests may include:
Skin biopsy—to look for abnormalities in the connective tissue
- Detection of specific biochemical defects—available for certain types of EDS
There is no known cure for EDS. Treatment may be needed to manage symptoms and or to try to prevent complications.
Treatment of Symptoms
Treatment will depend on your type of EDS and how severe it is.
For complications of the skin:
- Vitamin C supplements may be helpful in certain subtypes of EDS. It may help to decrease skin bruising and improve wound healing.
- Special care will be taken when repairing skin wounds. This may help to prevent or decrease scarring.
For musculoskeletal complications:
- Medication may help control pain.
- Surgery may be done to repair joint damage.
Some potential problems will need to be monitored. This includes patients at risk for blood vessel complications. Your doctor may ask for regular testing to examine major blood vessels.
Blood transfusions may be needed for severe bleeding.
Treatment to Reduce the Risk of Harm
Certain steps may help you reduce the chance of complications. The following may help you:
- Wear joint braces.
- Do muscle strengthening exercises.
- Consider physical therapy to help strengthen muscles and joints.
- Wear sunscreen daily.
- Avoid activities that may cause injury, bruising, or over-extending your joints.
- Children may be asked to wear protective gear during activity.
- Talk to your doctor about possible pregnancy complications.
There is no known way to prevent EDS after a person is born. If you have EDS or have a family history of the disorder, consider genetic counseling when deciding to have children. The counselor can talk to you about the risk of your child having EDS.