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Hypermobile Ehlers-Danlos Syndrome (a.k.a. Ehlers-Danlos Syndrome Type III and Ehlers-Danlos Syndrome Hypermobility Type) : Clinical Description and Natural History
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- Tinkle, Brad (author)
- Advocate Childrens Hosp, Clin Genet, Park Ridge, IL USA.
- Castori, Marco (author)
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- Berglund, Britta (author)
- Uppsala universitet,Institutionen för folkhälso- och vårdvetenskap
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- Advocate Childrens Hosp, Clin Genet, Park Ridge, IL USA Institutionen för folkhälso- och vårdvetenskap (creator_code:org_t)
- 2017-02-01
- 2017
- English.
- In: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. - : WILEY. - 1552-4868 .- 1552-4876. ; 175:1, s. 48-69
- Journal article (peer-reviewed)
Abstract
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- 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 manifestations-joint hypermobility syndrome and hEDS. Both are clinical diagnoses in the absence of other causation. Current medical literature further complicates differentiation and describes multiple associated symptoms and disorders. The current EDS nosology combines these two entities into the hypermobile type of EDS. Herein, we review and summarize the literature as a better clinical description of this type of connective tissue disorder.
Keyword
- joint hypermobility
- joint hypermobility syndrome
- Ehlers-Danlos syndrome type III
- Ehlers-Danlos syndrome hypermobility type
Publication and Content Type
- ref (subject category)
- art (subject category)
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- Tinkle, Brad
- Castori, Marco
- Berglund, Britta
- Cohen, Helen
- Grahame, Rodney
- Kazkaz, Hanadi
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- Levy, Howard
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