Ehlers-Danlos syndrome
Ehlers-Danlos syndrome (EDS) is a group of inherited disorders marked by extremely loose joints, very stretchy (hyperelastic) skin that bruises easily, and easily damaged blood vessels.
Hyperelastic
Hyperelastic skin is skin that can be stretched beyond what is considered normal. The skin returns to normal after it is stretched.
Read Article Now Book Mark ArticleCauses
There are at least 13 types of EDS.
A variety of gene changes (mutations) cause problems with collagen. This is the material that provides strength and structure to:
- Skin
- Bone
- Blood vessels
- Internal organs
The abnormal collagen leads to the symptoms associated with EDS. In some forms of the syndrome, the rupture of internal organs or abnormal heart valves can occur.
Family history is a risk factor in some cases.
Symptoms
Symptoms of EDS vary by type and may include:
- Back pain
- Double-jointedness
- Easily damaged, bruised, and stretchy skin
- Easy scarring and poor wound healing
- Flat feet
- Increased joint mobility, joints popping, early arthritis
- Joint dislocation
Joint dislocation
A dislocation is a disruption of the normal position of the ends of two or more bones where they meet at a joint. A joint is the place where two bon...
Read Article Now Book Mark Article - Joint pain
- Premature rupture of membranes during pregnancy
- Very soft and velvety skin
- Vision problems
Exams and Tests
Examination by a health care provider may show:
- Deformed surface of the eye (cornea)
- Excess joint looseness and joint hypermobility
Joint hypermobility
Hypermobile joints are joints that move beyond the normal range with little effort. Joints most commonly affected are the elbows, wrists, fingers, a...
Read Article Now Book Mark Article - Mitral valve in the heart does not close tightly (mitral valve prolapse)
Mitral valve prolapse
Mitral valve prolapse is a heart problem involving the mitral valve, which separates the upper and lower chambers of the left side of the heart. In ...
Read Article Now Book Mark Article - Gum infection (periodontitis)
Periodontitis
Periodontitis is inflammation and infection of the ligaments and bones that support the teeth.
Read Article Now Book Mark Article - Rupture of intestines, uterus, or eyeball (seen only in vascular EDS, which is rare)
- Soft, thin, or very stretchy skin
Tests to diagnose EDS include:
- Collagen typing (performed on a skin biopsy sample)
Skin biopsy
A skin lesion biopsy is when a small amount of skin is removed so it can be examined under a microscope. The skin is tested to look for skin conditi...
Read Article Now Book Mark Article - Collagen gene mutation testing
- Echocardiogram (heart ultrasound)
Echocardiogram
An echocardiogram is a test that uses sound waves to create pictures of the heart. The picture and information it produces is more detailed than a s...
Read Article Now Book Mark Article - Lysyl hydroxylase or oxidase activity (to check collagen formation)
Treatment
There is no specific cure for EDS. Individual problems and symptoms are evaluated and cared for appropriately. Physical therapy or evaluation by a doctor specializing in rehabilitation medicine is often needed.
Support Groups
More information and support for people with Ehlers-Danlos and their families can be found at:
The Ehlers-Danlos Society -- www.ehlers-danlos.com/support/
Outlook (Prognosis)
People with EDS generally have a normal life span. Intelligence is normal.
Those with the rare vascular type of EDS are at greater risk for rupture of a major organ or blood vessel. These people have a high risk for sudden death.
Possible Complications
Possible complications of EDS include:
- Chronic joint pain
- Early-onset arthritis
- Failure of surgical wounds to close (or stitches tear out)
- Premature rupture of membranes during pregnancy
- Rupture of major vessels, including a ruptured aortic aneurysm (only in vascular EDS)
Ruptured aortic aneurysm
The aorta is the main blood vessel that supplies blood to the abdomen, pelvis, and legs. An abdominal aortic aneurysm (AAA) occurs when an area of t...
Read Article Now Book Mark Article - Rupture of a hollow organ such as the uterus or bowel (only in vascular EDS)
- Rupture of the eyeball (only in vascular EDS)
When to Contact a Medical Professional
Contact your provider for an appointment if you have a family history of EDS and you are concerned about your risk or are planning to start a family.
Contact your provider for an appointment if you or your child has symptoms of EDS.
Prevention
Genetic counseling is recommended for prospective parents with a family history of EDS. Those planning to start a family should be aware of the type of EDS they have and how it is passed down to children. This can be determined through testing and evaluations suggested by your provider or genetic counselor.
Genetic counseling
Genetics is the study of heredity, the process of a parent passing certain genes on to their children. A person's appearance, such as height, hair co...
Read Article Now Book Mark ArticleIdentifying any significant health risks may help prevent severe complications by vigilant screening and lifestyle alterations.
Reviewed By
Jatin M. Vyas, MD, PhD, Associate Professor in Medicine, Harvard Medical School; Associate in Medicine, Division of Infectious Disease, Department of Medicine, Massachusetts General Hospital, Boston, MA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
Krakow D. Heritable diseases of connective tissue. In: Firestein GS, Budd RC, Gabriel SE, Koretzky GA, McInnes IB, O'Dell JR, eds. Firestein & Kelly's Textbook of Rheumatology. 11th ed. Philadelphia, PA: Elsevier; 2021:chap 111.
Pyeritz RE. Inherited diseases of connective tissue. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 26th ed. Philadelphia, PA: Elsevier; 2020:chap 244.