Hypermobility and Ehlers–Danlos syndromes
Syndroma Ehlers–Danlos (hypermobilitas articulorum) · Hypermobilita a Ehlersův–Danlosův syndrom
What it is
Faulty collagen makes joints too loose and skin stretchy; the hypermobile type is common and often missed for years.
Symptoms & signs
- Joints that bend too far and dislocate
- widespread pain and fatigue
- stretchy, fragile skin and easy bruising
- dizziness on standing (POTS)
- gut problems
🚩 Get help if…
- call 112 / 911 now Sudden severe pain in chest, belly or head (artery tear in vascular type)
- call 112 / 911 now Coughing blood or sudden breathlessness
- see a doctor soon Fainting or racing heart on standing
- see a doctor soon Joint that dislocates and won't go back
Where it strikes
Medical treatment
- Beighton score, and genetic tests for the rare types
- physiotherapy for joint stability
- pain management without long-term opioids
- treat POTS and gut symptoms
- vascular surveillance in vascular EDS (celiprolol)
Natural & lifestyle
- Low-impact strengthening (pilates, swimming)
- pacing
- braces and splints during flare-ups
Emerging & experimental
- Research into hypermobile EDS genes
- collagen-targeted therapies
Alternative, off-label & anecdotal
Approaches used outside the guidelines, with what their supporters report and what testing has found so far.
- Vitamin C — needed to build collagen; untested as treatment outside scurvy anecdotal / traditional
- Collagen supplements — popular; untested in EDS anecdotal / traditional
- Prolotherapy — case reports; risky in vascular EDS anecdotal / traditional
ICD codes
- ICD-10 Q79.6
- ICD-11 LD28.1Z Ehlers-Danlos syndrome, unspecified