Clinical characteristics of patients with hypermobile type Ehlers–Danlos syndrome (hEDS) and generalized hypermobility spectrum disorders (G-HSD): an online survey
Author:
Funder
Florida Physical Therapy Association.
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s00296-023-05378-3.pdf
Reference57 articles.
1. Palmer S et al (2016) Physiotherapy management of joint hypermobility syndrome—a focus group study of patient and health professional perspectives. Physiotherapy 102(1):93–102
2. Tinkle B, et al. (2017) Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): clinical description and natural history. Am J Med Genet C Semin Med Genet 175(1):48–69
3. Malfait F et al (2017) The 2017 international classification of the Ehlers–Danlos syndromes. Am J Med Genet C Semin Med Genet 175(1):8–26
4. Demmler JC et al (2019) Diagnosed prevalence of Ehlers–Danlos syndrome and hypermobility spectrum disorder in Wales, UK: a national electronic cohort study and case-control comparison. BMJ Open 9(11):e031365–e031365
5. Hakim AJ, Tinkle BT, Francomano CA (2021) Ehlers–Danlos syndromes, hypermobility spectrum disorders, and associated co-morbidities: reports from EDS ECHO. Am J Med Genet C Semin Med Genet 187(4):413–415
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