Ehlers-Danlos Syndrome (EDS)

Ehlers-Danlos Syndrome (EDS) is an assorted group of inherited connective tissue disorders characterized by joint hypermobility, stretchy skin and tissue fragility.  Collagen – a protein that acts as “glue” in the body by adding strength and elasticity to connective tissue – is faulty in those with EDS.

There are 6 major types of EDS that are classified according to their manifestations.  Each type is a distinct disorder passed on with a family.  Common symptoms include fragile skin that tears or bruises easily, severe scarring and loose and unstable joints, which are prone to frequent dislocations.  Pes planus feet (flat feet) are found in those with EDS.

Other names or similar foot conditions:

  • Familial joint hypermobility syndrome

Symptoms:

  • Fragile skin that tears or bruises easily
  • Slow wound healing and severe scarring
  • Loose and unstable joints prone to frequent dislocations
  • Joint pain

Signs to look for:

  • Diagnosis
  • History of joint dislocations
  • Flat feet

Possible Causes:

  • Genetic

Goals:

  • Align feet, ankles, knees and hips
  • Optimize balance
  • Provide arch support
  • Control motion in feet
  • Improve gait

How We Help:

Arch Supports:

Shoes:

Other:

Activities:

  • Regular exercise program that promotes increased strength and circulation in lower extremities
  • Regular stretching program for entire body
  • Rotation of weight bearing (such as walking) with non-weight bearing exercising (such as walking and swimming)

 

This information does not constitute a diagnosis of your condition and does not take the place of a doctor’s care.  The information has been compiled from sources available to the general public and referenced below.  Copyright 2005-2010  Carole Romig

Sources  Image:  Text: A. Decker, S. Albert, Contemporary Pedorthics, Ehler-Danlos.or

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