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Hypermobility

  • Hypermobility is common in healthy children. The term reflects an increase in range of movement and can be widespread or affect a small number of joints.
  • Hypermobility is more common in young children, females and certain ethnic populations (e.g., non-Caucasian children are generally more flexible than age-matched Caucasian children).
  • Many children will have no significant difficulties and it can be an advantage in certain situations (e.g., dancing, gymnastics).
  • A family history of hypermobility is common.
  • Hypermobility can present with the following:
    • Joint and muscle pain +/- transient joint swelling.
    • Clicking joints.
    • Fatigue.
    • Hand writing problems*.
    • Reduced co-ordination and balance*.
    • Flat feet.
    • Reduced general activity and function

*If these are predominant concerns then consider Developmental Co-ordination Disorder (DCD) 

  • Examination should include assessment of all joints (e.g., pGALS) where hypermobility is easily observed. e.g., hyperextension of fingers (pictures below), elbows or flat feet.
  • A knowledge of normal ranges of movement is useful.

The pictures below demonstrate Hypermobility - Hyperextension of elbows, thumb fully against the forearm, little finger, hands flat on the floor with spine flexed and hyperextension of the knees

  • Hypermobility is also a feature of the inherited collagen disorders - these are rare diseases which can cause complications in other systems e.g., cardiac and ocular. It is important to consider these as part of your differential diagnosis:
  • Management - Explanation and reassurance are important and often will suffice, with advice to maintain sporting activities and ensure good muscle strength and endurance with core stability optimised. Occasionally, advice from a paediatric physiotherapist can be useful, particularly in children struggling to return to normal activities, and especially if there is a history of recurrent dislocations. 
  • Patient information:

The photograph below shows blue sclerae suggesting osteogenesis imperfecta

The photograph below shows a paper thin scar in Ehler's Danlos syndrome

The photograph below shows elastic skin in Ehler's Danlos syndrome

Indications for concern and specialist opinion include:

  • Suspicion of inherited collagen syndromes (e.g., Marfans').
  • Pain and functional limitation.
  • Asymmetrical hypermobility. 
  • Inflammatory joint or muscle disease is suspected (remember children with arthritis may also have hypermobility!)
  • Recurrent dislocations.