What is Ehlers Danlos syndrome?

The Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that affect the connective tissues in the body. Connective tissue supports and connects different structures in the body, such as skin, joints, blood vessels and organs. In people with EDS, connective tissue is often less firm, which can lead to a wide range of symptoms. The condition is rare and varies greatly in severity and symptoms depending on the subtype. More info...

Ehlers-Danlos syndrome

What causes Ehlers-Danlos syndrome?

EDS is caused by genetic mutations that affect the production or structure of collagen. Collagen is an essential protein in connective tissue that provides strength and elasticity. Due to abnormalities in this protein, connective tissue in people with EDS is less functional, leading to the characteristic symptoms.

Heredity

  • EDS can be transmitted through an autosomal dominant or recessive manner, depending on the subtype.
  • Not all cases of EDS are hereditary; sometimes the mutation arises spontaneously.

What are the symptoms of Ehlers-Danlos syndrome?

Symptoms of EDS can vary widely depending on the subtype. Here are some general features that are common:

1. Hypermobility of joints

  • Joints move further than normal, often leading to instability, pain, and dislocations.
  • Excessive flexibility can improve athletic performance but increases the risk of injury.

2. Fragile and stretchy skin

  • The skin feels velvety soft and can easily stretch.
  • Wounds heal slowly and can leave wide scars.

3. Chronic pain and fatigue

  • Muscle and joint pain are common complaints.
  • Fatigue results from the extra effort required to stabilize the body.

4. Problems with blood vessels and organs (in certain subtypes)

  • Blood vessels can be fragile, which increases the risk of tearing.
  • Organs may become out of place (prolapse) or cause other complications.

5. Other symptoms

  • Excessive bruising.
  • Complaints of the gastrointestinal tract, such as reflux or constipation.
  • Problems with the autonomic nervous system, such as dizziness when standing up (POTS).

What are the subtypes of Ehlers-Danlos syndrome?

There are 13 recognized subtypes of EDS, each with unique characteristics and genetic causes. The most common are:

1. Hypermobile EDS (hEDS).

  • The most common subtype.
  • Characterized by joint hypermobility, chronic pain and fatigue.

2. Classical EDS (cEDS).

  • Stretchy and fragile skin, with conspicuous scars.
  • Often accompanied by joint instability.

3. Vascular EDS (vEDS).

  • The most severe subtype.
  • Blood vessels and organs are vulnerable to rupture, which can be life-threatening.

4. Kyphoscoliotic EDS (kEDS).

  • Characterized by severe back problems, such as curvature of the spine.
  • Weak muscles and brittle bones.

How is Ehlers-Danlos syndrome diagnosed?

The diagnosis is made based on a combination of clinical symptoms, medical history and genetic testing.

  1. Physical examination:

    • Assessment of joint hypermobility.
    • Checking for skin characteristics such as stretchiness and scarring.
  2. Genetic research:

    • Analysis to identify specific mutations.
    • This is especially important for the rarer subtypes.
  3. Assessment of family history:

    • Investigation of hereditary patterns in the family.

How is Ehlers-Danlos syndrome treated?

Although EDS cannot be cured, there are several ways to manage symptoms and improve quality of life:

1. Physiotherapy

  • Strengthens muscles and improves joint stability.
  • Helps prevent injuries and pain.

2. Pain Management

  • Use of medication or alternative therapies such as acupuncture.
  • Massage can relieve muscle tension, although caution should be used with fragile connective tissues.

3. Lifestyle modifications

  • Avoid activities that overload joints.
  • Use of braces or supportive devices to reduce instability.

4. Medical monitoring

  • Regular monitoring for complications, especially in vascular EDS.
  • Preventive measures to prevent damage to blood vessels and organs.

5. Psychological support

  • Living with EDS can be mentally challenging; therapy or support groups can help cope.

Can a massage chair such as MediRelaxa help with EDS?

Although EDS requires specific care, a MediRelaxa massage chair provide relief for some symptoms:

  • Muscle relaxation: Relieves muscle tension without stressing the joints.
  • Air compression: Gentle stimulation without pressure on delicate tissues.
  • Heat function: Promotes blood flow and reduces stiffness.

Important: Always consult with a doctor before using a massage chair, especially in severe forms of EDS.

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