What is Ehlers-Danlos Syndrome?

Ehlers-Danlos syndrome encompasses a group of inherited disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. The complex mixture of proteins and other substances that makes up connective tissue supplies underlying structures with tensile strength yet allows elasticity.

People with Ehlers-Danlos syndrome frequently have incredibly flexible joints and stretchy, delicate skin. When sutures are required for a wound, this could become problematic because the skin is often not strong enough to hold them in place.

A more severe form of the ailment is called vascular Ehlers-Danlos syndrome, and it can rupture the walls of your intestines, blood vessels, or uterus. You may want to discuss vascular Ehlers-Danlos syndrome with a genetic counselor before starting a family, as it may cause significant challenges during pregnancy.

What are the symptoms for Ehlers-Danlos syndrome?

Although the symptoms of each kind of Ehlers-Danlos syndrome vary, the following are the most common ones:

• Excessive flexibility or hypermobility of the joints can make them appear unstable or loose.
• Thinner, softer skin that stretches more than it should.
• Bruising more easily or frequently than usual.
• Aberrant scarring or an atypically protracted recovery time after a small cut or wound.
• Joint and muscular pains.
• Fatigue (the ongoing sensation of exhaustion).
• Unable to concentrate.

What is the cause of Ehlers-Danlos syndrome?

It is genetic mutation that causes Ehlers-Danlos syndrome. A genetic mutation is an alteration in a DNA sequence. It generally occurs at the time of division of cells, especially when your cells are copying. If some part of your DNA sequence is not in the correct place or if it is incomplete or even damaged, symptoms of a genetic condition may be experienced.

Even though we know it's caused by a genetic mutation, health care providers aren't always able to recognize exactly what that genetic mutation is that causes Ehlers-Danlos syndrome in a person.

To date, experts have identified over 20 different genetic mutations that can lead to Ehlers-Danlos syndrome. They all affect your body's ability to make collagen. Which specific mutation someone has determines which areas of the body will be affected.

What is the diagnosis for Ehlers-Danlos syndrome?

Your doctor will diagnose Ehlers-Danlos syndrome based on your medical history and a physical examination. He or she will also ask you about your symptoms and look at your skin and joints. Tell your doctor when your symptoms started and what you do that makes them worse.

Since most patients with Ehlers-Danlos syndrome do not have a known genetic mutation, the diagnosis of the disorder is generally based on medical history and symptoms expressed by the patient.

What is the treatment for Ehlers-Danlos syndrome?

Your health professional will be able to advise Ehlers-Danlos syndrome treatments that will help you to manage your symptoms and avoid serious possible complications. Course of treatment best for you depends on the EDS variety and, in turn on the severity of connective tissue involved.

Common Ehlers-Danlos syndrome treatments include:

• Application of sunscreen to protect the skin and mild soaps to clean.
• Physical therapy to strengthen the muscles that surround your joints.
• Wearing a brace to provide extra joint support.
• Individuals with Ehlers-Danlos syndrome are more likely to experience dislocated joints and other joint problems. As directed by your provider, avoid:
• Difficult (hefty) lifting.
• Intense exercise.
• Sports in which players make contact.

Is it possible to prevent Ehlers-Danlos syndrome?

The Ehlers-Danlos syndrome cannot be prevented. EDS cannot be prevented since you are powerless over the genetic changes that cause it. If you are concerned that your biological children may inherit EDS or any other genetic disorder, discuss genetic counseling with your healthcare physician.

Should I expect an Ehlers-Danlos syndrome diagnosis?

You should expect to live with the symptoms of Ehlers-Danlos syndrome for the rest of your life. There's no cure for EDS. But you should be able to resume all of your normal activities if you learn how to manage your symptoms. Avoiding physically demanding activities (such as contact sports) may be necessary for some types of exercise.

The effects of Ehlers-Danlos syndrome vary from person to person. What you experience depends depend on the severity of your symptoms and the kind of EDS you have. Ask your provider for a quote based on your own situation.

Whose life expectancy is affected by Ehlers-Danlos syndrome?

Most forms of Ehlers-Danlos syndrome do not affect your life expectancy.

A blood vessel-related form of EDS called vascular Ehlers-Danlos syndrome can increase your risk of stroke or other vascular problems that might be fatal.

Even with vascular Ehlers-Danlos syndrome, your health care provider will work with you to establish a course of action so you can live a safe, healthy life. Discuss things you need to know and warning signs and symptoms of possible serious complications with your physician .

Living With

How do I take care of myself?

Pay attention to your symptoms, and seek medical help if your symptoms improve or worsen. Your doctor will advise you on the frequency with which follow-up appointments are necessary to monitor changes in your body over time. They will modify the treatments as necessary.

Avoid high-impact sports- The more you engage in contact sports or another high-impact activity, the higher is the risk of joint injuries, especially dislocation.

Why Tender Palm Super-Speciality Hospital for Ehlers-Danlos syndrome treatment in Lucknow, India?

Tender Palm Super-Speciality Hospital is one of the best hospital for Ehlers-Danlos Syndrome treatment in Lucknow, India. We have expert team of vascular surgeons with modern technology, and compassionate care. We ensures safer surgeries, faster recovery, and better long-term results.

To seek an expert consultation for Ehlers-Danlos syndrome treatment in Lucknow, India:

Call us at +91-9076972161
Email at care@tenderpalm.com

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