Animal Models of Ehlers–Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential by Robin Vroman, Anne-Marie Malfait, Rachel E. Miller, Fransiska Malfait, Delfien Syx

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Social media use by patients with hypermobile Ehlers–Danlos syndrome by Colin M. E. Halverson, Tom A. Doyle, Samantha Vershaw

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Editorial: Neurodevelopmental, neuropsychiatric and psychosocial correlates of joint hypermobility and related disorders by Vincent Guinchat, Carolina Baeza-Velasco, Carolina Baeza-Velasco, Carolina Baeza-Velasco, Antonio Bulbena, Antonio Bulbena, Marco Castori

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Multifocal periapical cemental dysplasia in periodontal Ehlers–Danlos syndrome combined with leukoencephalopathy in the mutation of c.890G > a, G297D [pEDS] by Manfred Nilius, Minou Helene Nilius, Charlotte Müller, Guenter Lauer, Koch Berit, Kohlhaas Marcus

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Response to the Letter regarding “The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other... by Ricardo Gamboa, Maria Elena Soto

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Chinese Guidelines for Diagnosis and Treatment of the Ehlers-Danlos Syndromes by Chinese Multi-Disciplinary Working Group on the Ehlers-Danlos Syndromes

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Estimates of the excess cost burden of Ehlers-Danlos syndromes: a United States MarketScan® claims database analysis by Jane R. Schubart, Jane R. Schubart, Eric W. Schaefer, Dacre R. T. Knight, Susan E. Mills, Clair A. Francomano

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Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome by Emiko Okuda-Ashitaka, Ken-ichi Matsumoto

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Diagnosis and treatment of the Ehlers-Danlos syndromes in China: synopsis of the first guidelines by Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, On behalf of the Chinese Multi-Disciplinary Working Group on the Ehlers-Danlos Syndromes

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Progress in Clinical Diagnosis and Management of Short Stature in Ehlers-Danlos Syndromes by XU Kexin, LI Guozhuang, WU Zhihong, ZHANG Jianguo, DISCO(Deciphering Disorders Involving Scoliosis & Comorbidities) Study Group, WU Nan

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A qualitative study of pain and related symptoms experienced by people with Ehlers-Danlos syndromes by Jane R. Schubart, Susan E. Mills, Clair A. Francomano, Heather Stuckey-Peyrot

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Progress in Clinical Diagnosis and Management of Hypermobility Spectrum Disorders by XU Kexin, LI Guozhuang, WU Zhihong, DISCO (Deciphering Disorders Involving Scoliosis & COmorbidities) Study Group, ZHANG Jianguo, WU Nan

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Editorial: Research advances in understanding the etiology, epidemiology, pathophysiology, clinical features, and management of the Ehlers Danlos syndrome disorders by Clair A. Francomano, Anne Maitland, Deborah Krakow, Cheryl L. Maier

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Twin pregnancy with untyped Ehlers-Danlos syndrome requiring prompt genetic testing: A case report by Shiori Ogawa, Tasuku Mariya, Yuya Fujibe, Marie Ogawa, Keiko Ikeda, Miyako Mizukami, Yoshika Kuno, Aki Ishikawa, Shinichi Ishioka, Akihiro Sakurai, Tsuyoshi Saito

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Using social media listening to understand barriers to genomic medicine for those living with Ehlers–Danlos syndromes and hypermobility spectrum disorders by Erika Kline, Amanda Leigh Garrett, Catherine Brownstein, Sonja Ziniel, Erica Payton, Aleah Goldin, Kathleen Hoffman, Judy Chandler, Shani Weber

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Clinician-associated traumatization from difficult medical encounters: Results from a qualitative interview study on the Ehlers-Danlos Syndromes by Colin M.E. Halverson, Heather L. Penwell, Clair A. Francomano

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Advances in Clinical Genetics of the Ehlers-Danlos Syndromes by XU Kexin, LI Guozhuang, LI Qing, YIN Xiangjie, FANG Kun, WU Zhihong, ZHANG Jianguo, DISCO (Deciphering Disorders Involving Scoliosis ＆ COmorbidities) Study Group, WU Nan

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Oral Conditions and Oral Health-Related Quality of Life of People with Ehlers-Danlos Syndromes (EDS): A Questionnaire-Based Cross-Sectional Study by Marcel Hanisch, Moritz Blanck-Lubarsch, Lauren Bohner, Dominik Suwelack, Johannes Kleinheinz, Jeanette Köppe

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Physical activity and physical fitness in children with heritable connective tissue disorders by Lisanne de Koning, Lisanne de Koning, Jessica Warnink-Kavelaars, Jessica Warnink-Kavelaars, Marion van Rossum, Marion van Rossum, Selina Limmen, Ruth Van der Looven, Laura Muiño-Mosquera, Laura Muiño-Mosquera, Annelies van der Hulst, Jaap Oosterlaan, Jaap Oosterlaan, Lies Rombaut, Raoul Engelbert, Raoul Engelbert, Raoul Engelbert, on behalf of the Pediatric Heritable Connective Tissue Disorders Study Group

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Ballooning and Bursting of Barrels and Pipes: A Rare Case of Suspected Vascular Ehlers–Danlos Disease by Ogechi Agogbuo, Sri Harsha Kanuri, Luis Salinas, Mohamed Goweba, Khashayar Vahdat, Oscar Chastian, Larry Frase

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