Results 51 to 60 of about 2,102,167 (192)

Central sensitization as the mechanism underlying pain in joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type

, 2016
Patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type (JHS/EDS-HT) commonly suffer from pain. How this hereditary connective tissue disorder causes pain remains unclear although previous studies suggested it shares similar
A. Pepe, F. Camerota, G. Cruccu, LEONE, CATERINA, Celletti, C, Pepe, A, R. Baron, LA CESA, SILVIA, Baron, R, M. Di Franco, CRUCCU, Giorgio, A. Truini, DI STEFANO, GIULIA, Castori, M, M. Castori, S. La Cesa, G. Di Stefano, C. Celletti, DI FRANCO, Manuela, TRUINI, ANDREA, Camerota, F., C. Leone   +21 more
core   +1 more source

Venous insufficiency after prolonged standing: Is joint hypermobility an important risk factor?

Advanced Biomedical Research, 2015
Background: Varicose veins are extremely common disease which is due to elevated superficial venous pressures. We aimed to know that if joint hypermobility causes the venous insufficiency following the prolonged standing.
Kamran Azma, Peyman Mottaghi, Alireza Hosseini, Shadi Salek, Roya Bina   +4 more
doaj   +1 more source

Progress in Clinical Diagnosis and Management of Hypermobility Spectrum Disorders

罕见病研究, 2023
Joint hypermobility (JH) refers to the ability of joints to move beyond the 'normal' limits, which can be either physiologic or pathologic. Hypermobility spectrum disorders (HSDs) are a group of joint hypermobility-related clinical conditions.
XU Kexin, LI Guozhuang, WU Zhihong, DISCO (Deciphering Disorders Involving Scoliosis & COmorbidities) Study Group, ZHANG Jianguo, WU Nan   +5 more
doaj   +1 more source

Comparative diagnostic challenges in two horses with skin fragility disorders

Equine Veterinary Education, EarlyView.
Summary Hereditary equine regional dermal asthenia (HERDA) is an autosomal recessive connective tissue disorder of horses caused by a missense mutation (c.115G>A) in the peptidyl‐prolyl cis–trans isomerase B (PPIB) gene, resulting in defective collagen organisation.
M. Biolchi, F. A. Saiki, T. G. Cristo, M. C. Silva, R. J. Souza, A. F. Souza, R. A. Casagrande, J. H. Fonteque, C. I. G. Vogel   +8 more
wiley   +1 more source

Subjective health complaints and illness perception amongst adults with Joint Hypermobility Syndrome/Ehlers–Danlos Syndrome-HypermobilityType – a cross-sectional study [PDF]

, 2017
Objective: To investigate the prevalence and severity of subjective health complaints and describe illness perception in a population of Joint Hypermobility Syndrome or Ehlers–Danlos Syndrome-Hypermobile Type.
Lena Hope, Hope, Lena Maria, Løvaas, Helene, Løvvik, Camilla, Camilla Løvvik, Silje Maeland, Helene Løvaas, Juul-Kristensen, Birgit; id_orcid, Birgit Juul-Kristensen, Maeland, Silje   +9 more
core   +1 more source

The Assessment of the Occurrence of Benign Hypermobility Joint Syndrome in Physiotherapy Students

Central European Journal of Sport Sciences and Medicine, 2017
The occurrence of connective tissue disorders is an important factor for development of occupational diseases in professions requiring a non-ergonomic and often static load of the musculoskeletal system. Symptoms of the connective tissue disorders appear
Ewelina Żyżniewska-Banaszak, Hanna Tchórzewska-Korba, Magdalena Gębska, Katarzyna Weber Nowakowska, Katarzyna Leźnicka, Kuba Żyżniewski   +5 more
doaj   +1 more source

The Language of Pain in the Hypermobile Ehlers–Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation Tool

Brain Sciences, 2023
Ehlers–Danlos syndromes are a heterogeneous group of Heritable Connective Tissue Disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Filippo Camerota, Rachele Mariani, Giulia Cordiano, Michela Di Trani, Valentina Lodato, Alessandro Ferraris, Massimo Pasquini, Claudia Celletti   +7 more
doaj   +1 more source

Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study

Oral Diseases, EarlyView.
ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand, Benjamin P. J. Fournier, Grégoire Chevalier, Karelle Benistan, François Côme Ferré   +4 more
wiley   +1 more source

Prevalence of joint hypermobility, hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome in a university population: an observational study

, 2020
Objectives: To investigate the prevalence of joint hypermobility classes, hypermobility spectrum disorders,hypermobile Ehlers-Danlos syndrome and their relations with sex ina university population.
Filiz TUNA, Tuna, Filiz
core   +1 more source

Long COVID and hypermobility spectrum disorders have shared pathophysiology

Frontiers in Neurology
Hypermobility spectrum disorders (HSD) and hypermobile Ehlers–Danlos syndrome (hEDS) are the most common joint hypermobility conditions encountered by physicians, with hypermobile and classical EDS accounting for >90% of all cases.
Ravindra Ganesh, Bala Munipalli
doaj   +1 more source