Question 1

what is ehlers-danlos syndrome?

Accepted Answer

Extreme joint laxity: Ehlers-danlos syndrome is a group of inherited disorders marked by extremely loose joints, hyperelastic skin that bruises easily, and easily damaged blood vessels.

Question 2

how common is ehlers-danlos syndrome?

Accepted Answer

1 per 5,000: The combined incidence is estimate at one case per 5, 000 individuals.

Question 3

can ehlers-danlos syndrome get worse?

Accepted Answer

Yes it can: Because of the tendom laxicity, joints may not be as stable as normal joints. That can lead to increased risk of osteoarthritis particularly in larger joints such as the shoulder, hips, and knees. There may also be complications of chronic joint dislocation and chronic pain. The disease itself should not lead to any specific inflammatory diseases such as lupus or ra.

Question 4

what are the tests for ehlers-danlos syndrome?

Accepted Answer

Usually none: The diagnosis is usually made on physical examination.  Since it's not something that can be treated with a pill, there's seldom any need to find the exact gene responsible (and there are many different ones that can do it).  For the very severe vascular form, a geneticist may confirm this, before or after birth.  I know several docs with e-d.  Good luck.

Question 5

what kind of disease is ehlers-danlos syndrome?

Accepted Answer

Big answer: Ehlers-danlos syndrome is a group of diseases with characteristic joint laxity, very lax skin, easy bruising and weakened blood vessels.  There are several gene mutations for the various clinical pictures of this syndrome.  Beyond that i would suggest you research a more indepth answer online.

Question 6

what are the symptoms of ehlers-danlos syndrome?

Accepted Answer

Disorder of collagen: Ehlers-danlos syndrome is a common disorder of collagen structure that causes easy bruising and poor wound healing. Patients with this conditions have a soft, velvety skin that is hyperelastic, joins that are lax and they have unusual scarring.
There are 10 variants. The most serious form is associated with rupture of visceral organs.

Question 7

what re worst risks from ehlers-danlos syndrome?

Accepted Answer

Bone abnormalities: Low bone density from eds can lead to problems healing fractures and have joint pain. Spine deformities such as kyphosis or scoliosis can also occur. Irritiable bowel syndrome and GI disturbances can also be problemmatic. Finally, nerve compression syndromes such as carpal tunnel can occur along with known skin conditions, and blood disorders. Check with your physician to discuss fully.

Question 8

how does ehlers-danlos syndrome affect lifestyle?

Accepted Answer

Little effect: In the majority of cases, lifestyle is unaffected and most people with eds believe that everyone is as flexible as they are. Wound healing can be delayed, surgical suturing can be complicated, bruising may  be apparent; pregnancy can have complications. Some forms of arthritis are more common. Most people have no problems.

Question 9

has anyone heard of ehlers danlos syndrome causes?

Accepted Answer

Genetics: Ehlers-danlos is a genetic condition. There are no other known causes.

Question 10

how can you tell if you have ehlers danlos syndrome?

Accepted Answer

Ehlers Danlos: Symptoms of ehlers danlos include:
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 pain
premature rupture of membranes during pregnancy
very soft and velvety skin
vision problems.

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Ehlers danlos syndrome

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What is ehlers-danlos syndrome?

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What kind of disease is ehlers-danlos syndrome?

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Has anyone heard of ehlers danlos syndrome causes?

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