How are hypermobile EDS and hypermobility spectrum disorders diagnosed?
Hypermobile EDS and hypermobility spectrum disorders. Recently some changes were made to the way hypermobile Ehlers-Danlos syndrome is diagnosed. There is no test for hEDS, so diagnosis involves looking for joint hypermobility, signs of faulty connective tissue throughout the body (e.g. skin features, hernias, prolapses),…
How is hypermobile Ehlers Danlos syndrome ( hEDS ) diagnosed?
Recently some changes were made to the way hypermobile Ehlers-Danlos syndrome is diagnosed. There is no test for hEDS, so diagnosis involves looking for joint hypermobility, signs of faulty connective tissue throughout the body (e.g. skin features, hernias, prolapses),…
Can a person with HSD be hypermobile?
It is also possible to have been hypermobile in the past and to have gradually become stiffer with age, but still have the musculosketal issues associated with that historical hypermobility. HSD are likely to be common. Someone with HSD can be just as symptomatic, more so even, than someone with hEDS.
Is the treatment for HSD the same as Ehlers Danlos?
Management advice for both hEDS and HSD is the same. Dr Kazkaz talks about the history of the Ehlers-Danlos syndromes, right up to the most recent 2017 reclassification. The genetics behind connective tissue, heritable disorders of connective tissue and the different types of EDS.
What is the cause of hypermobile Ehlers Danlos syndrome?
Try our interactive tool for help finding information, services, experts, financial aid, and more! Hypermobile Ehlers-Danlos syndrome is an inherited connective tissue disorder that is caused by defects in a protein called collagen.
Is there a difference between benign joint hypermobility syndrome and EDS?
The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities. There is still debate as to whether benign joint hypermobility syndrome (BJHS) is a distinct disorder or part of a clinical continuum.