Ehlers-Danlos syndromes are rare hereditary disorders of connective tissue that result in unusually flexible joints, very elastic skin, and fragile tissues.
These syndromes are caused by a defect in one of several genes that control the production of connective tissue.
Typical symptoms include flexible joints, a humpback, flat feet, and elastic skin.
The diagnosis is based on symptoms and results of a physical examination.
Most people with this syndrome have a normal life span.
There is no cure for Ehlers-Danlos syndromes.
Ehlers-Danlos syndromes are caused by an abnormality in one of the genes that controls the production of connective tissue. Connective tissue is the tough, often fibrous tissue that binds the body's structures together and provides support and elasticity.
There are 6 major types of Ehlers-Danlos syndrome and 7 less common types. They involve different genes and vary widely in severity. Although the types have slightly different symptoms, they all result in abnormally fragile connective tissue, which causes problems in joints and bones and may weaken internal organs.
Dalili za Magonjwa ya Ehlers-Danlos
ST MARYS HOSPITAL MEDICAL SCHOOL/SCIENCE PHOTO LIBRARY
People with an Ehlers-Danlos syndrome usually have very flexible joints, abnormal scarring, poor wound healing, fragile blood vessels, and very elastic skin. The skin can be stretched up to several inches but returns to its normal position when released.
Some people develop small, hard, round lumps under the skin.
In a small number of people, the blood does not clot normally, so bleeding from minor wounds may be difficult to stop.
Matatizo ya Magonjwa ya Ehlers-Danlos
Ehlers-Danlos syndromes may alter the body’s response to injuries. Minor injuries may result in wide gaping wounds. Although these wounds usually do not bleed excessively, they leave wide scars.
Sprains and dislocations develop frequently.
Some people develop a chest deformity, a humpback with an abnormal curve of the spine (kyphoscoliosis), or a clubfoot.
Most adults have flat feet.
The intestines can bulge through the abdominal wall (called a hernia), and abnormal outpouchings (diverticula) can develop in the intestine. Rarely, a fragile intestine bleeds or ruptures (perforates—see Perforation of the Digestive Tract).
Sometimes weak tissue in a heart valve causes the valve to leak.
If a pregnant woman has an Ehlers-Danlos syndrome, delivery may be premature. The mother's fragile tissues increase risk that her uterus may rupture during labor. Poor skin healing may make an episiotomy or cesarean delivery (C-section) problematic. If the fetus has an Ehlers-Danlos syndrome, the amniotic sac may rupture early (prelabor rupture of membranes). A mother or baby who has an Ehlers-Danlos syndrome can bleed excessively before, during, and after delivery.
Utambuzi wa Magonjwa ya Ehlers-Danlos
A doctor's evaluation
Genetic testing
Skin biopsy
Imaging tests to detect complications
A doctor bases the diagnosis of an Ehlers-Danlos syndrome on the symptoms and results of a physical examination.
To confirm the diagnosis, genetic tests are usually done.
The doctor can identify some of the types of Ehlers-Danlos syndrome by taking a sample of skin to examine under a microscope (biopsy).
Other tests are done to check for conditions that are associated with complications. For example, echocardiography and other imaging tests are usually done to detect problems with the heart or blood vessels.
Utabiri wa Magonjwa ya Ehlers-Danlos
Despite the many and varied complications people with an Ehlers-Danlos syndrome may have, their life span is usually normal.
However, potentially fatal complications (usually bleeding) occur in certain types.
Matibabu ya Magonjwa ya Ehlers-Danlos
Injury prevention
There is no way to cure an Ehlers-Danlos syndrome or to correct the abnormalities in the connective tissue.
Injuries can be treated, but it may be difficult for a doctor to stitch cuts because stitches tend to tear out of the fragile tissue. Usually, using an adhesive tape or medical skin glue closes cuts more easily and leaves less scarring.
Special precautions should be taken to prevent injuries. For example, children with severe forms of Ehlers-Danlos syndromes can wear protective clothing and padding.
Surgery requires special techniques that minimize injury and ensure that a large supply of blood is available for transfusion.
An obstetrician (a doctor who specializes in childbirth and in caring for and treating women who are giving birth) must supervise pregnancy and delivery.
Genetic counseling for family members is suggested.
