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Ehlers-Danlos syndrome (EDS) is an inherited condition that affects the connective tissues in the body. Connective tissue is responsible for supporting and structuring the skin, blood vessels, bones, and organs. It’s made up of cells, fibrous material, and a protein called collagen. Ehlers-Danlos syndrome is caused by a defect in collagen production. This condition is caused by a group of genetic disorders.
There are six major types of Ehlers-Danlos syndrome:
The area affected differs with each type of EDS. However, they all have one thing in common: hypermobility. Hypermobility is an unusually large range of movement in the joints.
The hypermobility and classic types of Ehlers-Danlos syndrome are the most common. The other types are rare, with the dermatosparaxis type affecting only about a dozen children on record worldwide. According to the National Library of Medicine’s Genetics Home Reference, EDS is seen in 1 in 5,000 people worldwide.
EDS is, in most cases an inherited condition, while a minority of cases are not inherited (meaning that they occur via spontaneous gene mutations).
Defects in the following genes cause EDS. All of these genes provide instructions on how to assemble collagen — except for ADAMTS2, which provides instructions for making the proteins that work with collagen.
Defects in these genes weaken the process and formation of collagen. Collagen is made up of molecules that give structure to connective tissues in the body.
Parents are often silent carriers of the defective gene that causes EDS. This means the parents may not show any signs of the condition, and are unaware that they are carriers of the defective gene. Symptoms of classic EDS are:
Symptoms of hypermobility EDS are:
Symptoms of vascular EDS are:
A series of tests may be used to diagnose EDS. They include genetic tests, skin biopsy, and echochardiogram. An echocardiogram uses sound waves to create moving images of the heart. This will show the doctor if there are any abnormalities present.
A blood sample is taken from your arm and tested for mutations in certain genes. A DNA test can confirm if the gene is present in embryos as well. This form of testing is done when the woman’s eggs are fertilized outside of her body (in vitro fertilization).
A skin biopsy is used to check for signs of abnormalities in collagen production. This is performed by removing a small sample of skin and checking it under a microscope.
Current treatment options for EDS include:
Additional treatment options may be available depending on the amount of pain you are experiencing or any additional symptoms.
Take these steps to prevent injuries and to protect your joints:
Complications of EDS may include:
Written by: April Kahn
Published on: Aug 04, 2015
Medically reviewed on: Aug 31, 2017: Daniel Murrell, MD
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