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Ehlers Danlos Syndrome (EDS)

What is Ehlers Danlos Syndrome?
The Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders that are frequently characterized by:
  • Flexible joints
  • Pale skin & veins
  • Stretchy, fragile skin
  • Tissue fragility with poor wound healing
  • Easy bruising
​What are the 13 subtypes of EDS?
  • Hypermobile (most common)
  • Classical
  • Vascular
  • Periodontal
  • Kyphoscolitoic
  • Spondylodysplastic Ehlers-Danlos Syndrome (spEDS)
  • Brittle Cornea Syndrome
  • Arthrochalasia Ehlers-Danlos Syndrome (aEDS)
  • Musculocontractural Ehlers-Danlos Syndrome (mcEDS)
  • Classical-Like EDS
  • Dermatosparaxis Ehlers-Danlos Syndrome (dEDS)
  • Myopathic
  • Cardiac-Vulvular
What causes EDS?
The conditions are thought to be caused by genetic changes that affect connective tissue; however, there are different theories as to how EDS is caused. 
  • Specific genetic mutations
  • RCCX Theory
  • MCAS or a MCAS-degranulating, post-viral event like COVID
How is EDS diagnosed?
Because the hyper-mobile subtype is the most common, and it is the only subtype for which a mutation has not been conclusively identified, diagnosis at this moment is still based on clinical symptoms and findings; however, that is likely to change soon given the Norris lab has recently identified a genetic mutation called KLK15 that they believe may be responsible for some hEDS.
 Here's the checklist for hEDS
How can EDS be treated?
  • Dr. Bluestein's Holistic Approach
  • Dr. Zingman's Prism approach
  • Prolotherapy, PRP and Regenerative Medicine Treatment for EDS
  • The Muldowney Protocol for PT with EDS
Where can I learn more?
  • What is EDS? by the Ehlers Danlos Society
  • The link between EDS, MCAS & POTS by Dr. Weinstock, a GI




















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  • Learn
    • Genetics
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    • EDS
    • MCAS
    • POTS
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    • Cusack Protocol
  • Resources
    • Hypermobility Hacks
    • Info Resources
    • Treatment
  • Contact