Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history
Volume: 175, Issue: 1, Pages: 48 - 69
Published: Feb 1, 2017
Abstract
The hypermobile type of Ehlers–Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissue. It has been described largely in those with musculoskeletal complaints including joint hypermobility, joint subluxations/dislocations, as well as skin and soft tissue manifestations. Many patients report activity‐related pain and some go on to have daily pain. Two undifferentiated syndromes have been used to describe these...
Paper Details
Title
Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history
Published Date
Feb 1, 2017
Volume
175
Issue
1
Pages
48 - 69
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