Results 51 to 60 of about 3,078 (199)

Are patients with hypermobile Ehlers-Danlos syndrome or hypermobility spectrum disorder so different? [PDF]

, 2021
Diagnosing hypermobile Ehlers-Danlos syndrome (hEDS) remains challenging, despite new 2017 criteria. Patients not fulfilling these criteria are considered to have hypermobile spectrum disorder (HSD).
Aubry-Rozier, B., Benaim, C., Berna, C., Hügle, T., Paquier, C., Schwitzguebel, A., Tanniger, J., Valerio, F.   +7 more
core   +1 more source

Pediatric joint hypermobility: a diagnostic framework and narrative review

Orphanet Journal of Rare Diseases, 2023
Background Hypermobile Ehlers–Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are debilitating conditions. Diagnosis is currently clinical in the absence of biomarkers, and criteria developed for adults are difficult to use in children ...
Louise Jane Tofts, Jane Simmonds, Sarah B. Schwartz, Roberto M. Richheimer, Constance O’Connor, Ellen Elias, Raoul Engelbert, Katie Cleary, Brad T. Tinkle, Antonie D. Kline, Alan J. Hakim, Marion A. J. van Rossum, Verity Pacey   +12 more
doaj   +1 more source

Desmoid Fibromatosis Presenting with Gastrointestinal Manifestations in a Patient with Ehlers-Danlos Syndrome: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Ehlers-Danlos syndrome comprises 13 hereditary connective tissue disorders associated with skin hyperelasticity, joint hypermobility, atrophic scarring, and blood vessel fragility.
Elias Lugo-Fagundo, Edmund M Weisberg, Ryan C Rizk, Elliot K Fishman   +3 more
doaj   +1 more source

Mechanobiology in the Comorbidities of Ehlers Danlos Syndrome

Frontiers in Cell and Developmental Biology, 2022
Ehlers-Danlos Syndromes (EDSs) are a group of connective tissue disorders, characterized by skin stretchability, joint hypermobility and instability. Mechanically, various tissues from EDS patients exhibit lowered elastic modulus and lowered ultimate ...
Shaina P. Royer, Sangyoon J. Han, Sangyoon J. Han, Sangyoon J. Han   +3 more
doaj   +1 more source

Síndroma de Ehlers-Danlos – Uma causa rara de pneumotórax espontâneo

Revista Portuguesa de Pneumologia, 2006
Resumo: A síndroma de Ehlers-Danlos (cutis hyperelastica), constitui uma patologia do tecido conjuntivo caracterizada por alterações da pele, ligamentos e órgãos internos.Apresenta transmissão hereditária, em geral autossómica dominante.
Carlos Lopes, Alda Manique, Renato Sotto-Mayor, Jorge Cruz, Margarida Mendes de Almeida, João Cravino, A Bugalho de Almeida   +6 more
doaj   +1 more source

The effectiveness of a multidisciplinary intervention strategy for the treatment of symptomatic joint hypermobility in childhood:A randomised, single Centre parallel group trial (The Bendy Study) [PDF]

, 2019
Introduction: Joint hypermobility is common in childhood and can be associated with musculoskeletal pain and dysfunction. Current management is delivered by a multidisciplinary team, but evidence of effectiveness is limited.
A Bulbena, A Hakim, A Qvindesland, AG Canaway, Alex J. MacGregor, Allan Clark, AU Qureshi, B Smits-Engelsman, BL Loeys, Emma Jerman, F Malfait, G Garra, G Singh, Garry Barton, Holly Bacon, J Clinch, J Inocencio Arocena de, JC Cheng, K Stevens, K Stevens, Kate Armon, L Frohlich, Laura Watts, M Castori, M McCormack, MC Scheper, MM Schoemaker, MR Simpson, N Sahin, NM Lamari, P Beighton, P Beighton, Peter Bale, RH Engelbert, RH Engelbert, RP Hasija, S Kemp, SE Henderson, U Seçkin, V Easton, Vicky Easton   +40 more
core   +1 more source

Arthralgias, fatigue, paresthesias and visceral pain: can joint hypermobility solve the puzzle? A case report [PDF]

, 2016
Background: Joint hypermobility syndrome describes a disorder in which musculoskeletal pain occurs in a generalized joint hypermobility substrate.
Franco Capsoni, Marco Folci
core   +2 more sources

Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type [PDF]

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017
Autonomic dysfunction contributes to health‐related impairment of quality of life in the hypermobile type of Ehlers–Danlos syndrome (hEDS). Typical signs and symptoms include tachycardia, hypotension, gastrointestinal dysmotility, and disturbed bladder function and sweating regulation.
Alan, Hakim, Chris, O'Callaghan, Inge, De Wandele, Lauren, Stiles, Alan, Pocinki, Peter, Rowe   +5 more
openaire   +2 more sources

Clinician-associated traumatization from difficult medical encounters: Results from a qualitative interview study on the Ehlers-Danlos Syndromes

SSM: Qualitative Research in Health, 2023
Patients with hypermobile Ehlers Danlos Syndrome often experience psychological distress resulting from the perceived hostility and disinterest of their clinicians.
Colin M.E. Halverson, Heather L. Penwell, Clair A. Francomano   +2 more
doaj   +1 more source

A humanisation approach for the management of Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobility Type (JHS/EDS-HT). [PDF]

, 2017
Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobility Type (JHS/EDS-HT) is a complex and multisystemic condition which significantly impacts on a person's health and well-being and is challenging for health professionals (HPs) to manage ...
Carol J. Clark, Clark C. J., Connelly E., Farmer A., Grahame R., Isobel Knight, Knight I., Nielsen A., Nielsen M., Peterkin A.   +9 more
core   +1 more source